chr5:112176115:ACCA>TAC 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	chr5:112,176,115-112,176,118
hg38	chr5:112,840,418-112,840,421 View the variant detail on this assembly version.

HGVS

APC

Type	Transcript	Protein
RefSeq	NM_000038.5:c.4824_4827delinsTAC	NP_000029.2:p.Lys1608AsnfsTer42
	NM_001127511.2:c.4770_4773delinsTAC	NP_001120983.2:p.Lys1590AsnfsTer42
	NM_001127510.2:c.4824_4827delinsTAC	NP_001120982.1:p.Lys1608AsnfsTer42
Ensemble	ENST00000257430.9:c.4824_4827delinsTAC	ENST00000257430.9:p.Lys1608AsnfsTer42
	ENST00000504915.3:c.4878_4881delinsTAC	ENST00000504915.3:p.Lys1626AsnfsTer42
	ENST00000507379.6:c.4770_4773delinsTAC	ENST00000507379.6:p.Lys1590AsnfsTer42
	ENST00000508376.6:c.4824_4827delinsTAC	ENST00000508376.6:p.Lys1608AsnfsTer42
	ENST00000509732.6:c.4824_4827delinsTAC	ENST00000509732.6:p.Lys1608AsnfsTer42
	ENST00000512211.7:c.4824_4827delinsTAC	ENST00000512211.7:p.Lys1608AsnfsTer42
	ENST00000713638.1:c.2806_2809delinsTAC
	ENST00000713639.1:c.4506_4509delinsTAC	ENST00000713639.1:p.Lys1502AsnfsTer42

Summary

MGeND

Clinical significance
Variant entry
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
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2014-06-27	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2019-01-26	criteria provided, single submitter	familial adenomatous polyposis 1	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.121	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000038.6(APC):c.4824_4827delinsTAC (p.Lys1608fs) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000038.6(APC):c.4824_4827delinsTAC (p.Lys1608fs) AND Familial adenomatous polyposis 1	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: rs786202276 dbSNP
Genome: hg19
Position: chr5:112,176,115-112,176,118
Variant Type: snv
Reference Allele: ACCA
Alternative Allele: TAC

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