chr5:112173704:C>T Detail (hg19) (APC)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr5:112,173,704-112,173,704
hg38	chr5:112,838,007-112,838,007 View the variant detail on this assembly version.

HGVS

APC

Type	Transcript	Protein
RefSeq	NM_000038.5:c.2413C>T	NP_000029.2:p.Arg805Ter
	NM_001127510.2:c.2413C>T	NP_001120982.1:p.Arg805Ter
	NM_001127511.2:c.2359C>T	NP_001120983.2:p.Arg787Ter
Ensemble	ENST00000257430.9:c.2413C>T	ENST00000257430.9:p.Arg805Ter
	ENST00000508376.6:c.2413C>T	ENST00000508376.6:p.Arg805Ter
	ENST00000504915.3:c.2467C>T	ENST00000504915.3:p.Arg823Ter
	ENST00000507379.6:c.2359C>T	ENST00000507379.6:p.Arg787Ter
	ENST00000509732.6:c.2413C>T	ENST00000509732.6:p.Arg805Ter
	ENST00000512211.7:c.2413C>T	ENST00000512211.7:p.Arg805Ter
	ENST00000713638.1:c.*395C>T
	ENST00000713639.1:c.2095C>T	ENST00000713639.1:p.Arg699Ter

Summary

MGeND

Clinical significance	not provided
Variant entry	11
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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Links

APC

Type	Database	ID	Link
Gene	MIM	611731	OMIM
	HGNC	583	HGNC
	Ensembl	ENSG00000134982	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM19058	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
not provided		pyloric antrum	not provided	MGS000041 (TMGS000094)	Hitoshi Nakagama	National Cancer Center Japan
not provided		caecum	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		colon, unspecified	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
not provided		colorectal cancer	somatic	MGS000018 (TMGS000110)	Hitoshi Nakagama	National Cancer Center Japan	30742731

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2022-03-21	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2021-10-15	criteria provided, multiple submitters, no conflicts	Familial multiple polyposis syndrome	germline	Detail
Pathogenic	2019-10-01	criteria provided, single submitter	not provided	germline	Detail
Pathogenic	2020-10-15	criteria provided, single submitter	Desmoid disease, hereditary	de novo	Detail
not provided		no assertion provided	APC-related attenuated familial adenomatous polyposis,Gastric adenocarcinoma and proximal polyposis of the stomach,familial adenomatous polyposis 1	unknown	Detail
not provided		no assertion provided	APC-related attenuated familial adenomatous polyposis,Gastric adenocarcinoma and proximal polyposis of the stomach,familial adenomatous polyposis 1	unknown	Detail
not provided		no assertion provided	APC-related attenuated familial adenomatous polyposis,Gastric adenocarcinoma and proximal polyposis of the stomach,familial adenomatous polyposis 1	unknown	Detail
Pathogenic	2023-10-04	criteria provided, multiple submitters, no conflicts	familial adenomatous polyposis 1	germline unknown	Detail
Pathogenic	2024-01-03	criteria provided, single submitter	APC-related disorder	germline	Detail
Pathogenic	2023-07-09	criteria provided, single submitter	Classic or attenuated familial adenomatous polyposis	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.121	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail
0.120	Polyposis, Adenomatous Intestinal	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND Familial multiple polyposis syndrome	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND not provided	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND Desmoid disease, hereditary	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND multiple conditions	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND multiple conditions	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND multiple conditions	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND Familial adenomatous polyposis 1	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND APC-related disorder	ClinVar	Detail
NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND Classic or attenuated familial adenomatous polyposis	ClinVar	Detail
NA	DisGeNET	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: rs587779783 dbSNP
Genome: hg19
Position: chr5:112,173,704-112,173,704
Variant Type: snv
Reference Allele: C
Alternative Allele: T

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