chr17:7574003:G>A Detail (hg19) (TP53)

Information

Genome

Assembly Position
hg19 chr17:7,574,003-7,574,003
hg38 chr17:7,670,685-7,670,685 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_001126113.2:c.*43C>T
NM_001276695.1:c.*43C>T
NM_001126116.1:c.*131C>T
Summary

MGeND

Clinical significance Pathogenic not provided
Variant entry 123
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 191170 OMIM
HGNC 11998 HGNC
Ensembl ENSG00000141510 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM11073 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Pathogenic 2020/04/20 bronchus or lung, unspecified not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 lower third of oesophagus not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 fundus of stomach not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 body of stomach not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 pyloric antrum not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 caecum not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 ascending colon not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 descending colon not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 sigmoid colon not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 colon, unspecified not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 malignant neoplasm of rectosigmoid junction not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 malignant neoplasm of rectum not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 extrahepatic bile duct not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 head of pancreas not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 ill-defined sites within the digestive system not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2019/03/05 mediastinum germline MGS000029
(TMGS000133)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2019/03/05 malignant neoplasm of thyroid gland germline MGS000029
(TMGS000133)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2019/03/05 breast, unspecified germline MGS000029
(TMGS000133)
Hitoshi Nakagama National Cancer Center Japan
not provided Myelodysplastic syndromes somatic MGS000005
(TMGS000006)
Keizo Horibe National Hospital Organization Nagoya Medical Center
Pathogenic Primary adenocarcinoma of colon (disorder) unknown MGS000021
(TMGS000080)
Manabu Muto Kyoto University
Pathogenic Neoplasm of ovary (disorder) unknown MGS000022
(TMGS000081)
Manabu Muto Kyoto University
Pathogenic Sarcoma of uterus (disorder) unknown MGS000025
(TMGS000084)
Manabu Muto Kyoto University
not provided Hepatocellular carcinoma somatic MGS000018
(TMGS000110)
Hitoshi Nakagama National Cancer Center Japan 30742731
not provided Bone sarcoma germline MGS000018
(TMGS000110)
Hitoshi Nakagama National Cancer Center Japan 30742731
not provided pancreatic cancer somatic MGS000018
(TMGS000110)
Hitoshi Nakagama National Cancer Center Japan 30742731
Pathogenic 2020/04/20 body of stomach not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 small intestine, unspecified not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 caecum not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 ascending colon not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 descending colon not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 sigmoid colon not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 colon, unspecified not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 malignant neoplasm of rectosigmoid junction not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 malignant neoplasm of rectum not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 extrahepatic bile duct not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 head of pancreas not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 bronchus or lung, unspecified not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 middle third of oesophagus not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 lower third of oesophagus not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 fundus of stomach not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 body of stomach not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 caecum not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 descending colon not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 colon, unspecified not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 malignant neoplasm of rectosigmoid junction not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 extrahepatic bile duct not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
Pathogenic 2020/04/20 head of pancreas not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2022-06-18 criteria provided, multiple submitters, no conflicts Hereditary cancer-predisposing syndrome germline Detail
Pathogenic 2022-03-31 criteria provided, multiple submitters, no conflicts not provided germline Detail
Pathogenic 2024-03-25 criteria provided, multiple submitters, no conflicts Li-Fraumeni syndrome germline Detail
Pathogenic 2018-12-01 no assertion criteria provided Neoplasm of ovary somatic Detail
Pathogenic 2020-10-30 no assertion criteria provided gallbladder cancer somatic Detail
Pathogenic 2021-08-09 no assertion criteria provided germline Detail
Pathogenic 2024-02-21 criteria provided, multiple submitters, no conflicts Li-Fraumeni syndrome 1 germline unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2021-07-14 criteria provided, single submitter Basal cell carcinoma, susceptibility to, 7,Adrenocortical carcinoma, hereditary,hepatocellular carcinoma,Bone marrow failure syndrome 5,Glioma susceptibility 1,Li-Fraumeni syndrome 1,colorectal cancer,choroid plexus papilloma,Familial cancer of breast,Carcinoma of pancreas,bone osteosarcoma,Nasopharyngeal carcinoma unknown Detail
Pathogenic 2022-10-28 criteria provided, single submitter Adrenocortical carcinoma, hereditary unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.122 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND not provided ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Li-Fraumeni syndrome ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Neoplasm of ovary ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Gallbladder cancer ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Colonic diverticula ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Li-Fraumeni syndrome 1 ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND multiple conditions ClinVar Detail
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter) AND Adrenocortical carcinoma, hereditary ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs730882029 dbSNP
Genome
hg19
Position
chr17:7,574,003-7,574,003
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser