chr17:7577570:C>T Detail (hg19) (TP53)

Information

Genome

Assembly Position
hg19 chr17:7,577,570-7,577,570
hg38 chr17:7,674,252-7,674,252 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_001126116.1:c.315G>A NP_001119588.1:p.Met105Ile
NM_001276698.1:c.315G>A NP_001263627.1:p.Met105Ile
NM_000546.5:c.711G>A NP_000537.3:p.Met237Ile
Summary

MGeND

Clinical significance not provided
Variant entry 36
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

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 COSM3378348 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided bronchus or lung, unspecified not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
not provided fundus of stomach not provided MGS000040
(TMGS000095) 		Hitoshi Nakagama National Cancer Center Japan
not provided descending colon not provided MGS000040
(TMGS000095) 		Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectosigmoid junction not provided MGS000040
(TMGS000095) 		Hitoshi Nakagama National Cancer Center Japan
not provided ill-defined sites within the digestive system not provided MGS000040
(TMGS000095) 		Hitoshi Nakagama National Cancer Center Japan
not provided Myelodysplastic syndromes somatic MGS000005
(TMGS000006) 		Keizo Horibe National Hospital Organization Nagoya Medical Center
not provided 2018/05/15 stomach neoplasms somatic MGS000017
(TMGS000034) 		Kohei Miyazono Tokyo University
not provided Renal cell carcinoma (Bellini duct carcinoma) somatic MGS000018
(TMGS000110) 		Hitoshi Nakagama National Cancer Center Japan 30742731
not provided fundus of stomach not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided body of stomach not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided pyloric antrum not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided transverse colon not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectosigmoid junction not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectum not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided ill-defined sites within the digestive system not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided bronchus or lung, unspecified not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
not provided body of stomach not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
not provided stomach, unspecified not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
not provided descending colon not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectosigmoid junction not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectum not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2022-11-28 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Neoplasm of brain somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided ovarian serous cystadenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Malignant neoplasm of body of uterus somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Squamous cell carcinoma of the head and neck somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Carcinoma of esophagus somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided lung adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided gastric adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Breast neoplasm somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided pancreatic adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Neoplasm of the large intestine somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Squamous cell lung carcinoma somatic Detail
Likely pathogenic 2023-12-04 criteria provided, single submitter Li-Fraumeni syndrome germline Detail
Uncertain significance no assertion criteria provided not specified unknown Detail
Likely pathogenic 2018-12-01 no assertion criteria provided Neoplasm of ovary somatic Detail
Likely pathogenic 2019-06-11 no assertion criteria provided Breast and/or ovarian cancer germline Detail
Pathogenic 2021-04-20 reviewed by expert panel Li-Fraumeni syndrome 1 germline unknown Detail
Pathogenic 2020-04-15 criteria provided, single submitter not provided germline Detail
Pathogenic 2023-09-23 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.711G>A (p.Met237Ile) AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Neoplasm of brain ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Ovarian serous cystadenocarcinoma ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Malignant neoplasm of body of uterus ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Brainstem glioma ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Squamous cell carcinoma of the head and neck ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Carcinoma of esophagus ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Lung adenocarcinoma ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Gastric adenocarcinoma ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Breast neoplasm ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Pancreatic adenocarcinoma ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Neoplasm of the large intestine ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Squamous cell lung carcinoma ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Li-Fraumeni syndrome ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND not specified ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Neoplasm of ovary ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Breast and/or ovarian cancer ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND Li-Fraumeni syndrome 1 ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) AND not provided ClinVar Detail
NM_000546.6(TP53):c.711G>A (p.Met237Ile) 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
rs587782664 dbSNP
Genome
hg19
Position
chr17:7,577,570-7,577,570
Variant Type
snv
Reference Allele
C
Alternative Allele
T
East Asian Chromosome Counts (ExAC)
8652
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
121356
Allele Counts in All Race (ExAC)
1
Heterozygous Counts in All Race (ExAC)
1
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
8.240218860212928E-6
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