chr5:112838756:C> Detail (hg38) (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	chr5:112,174,453-112,174,453
hg38	chr5:112,838,756-112,838,756

HGVS

APC

Type	Transcript	Protein
RefSeq	NM_000038.5:c.3162delC	NP_000029.2:p.His1054GlnfsTer2
	NM_001127511.2:c.3108delC	NP_001120983.2:p.His1036GlnfsTer2
	NM_001127510.2:c.3162delC	NP_001120982.1:p.His1054GlnfsTer2
Ensemble	ENST00000257430.9:c.3162delC	ENST00000257430.9:p.His1054GlnfsTer2
	ENST00000504915.3:c.3216delC	ENST00000504915.3:p.His1072GlnfsTer2
	ENST00000507379.6:c.3108delC	ENST00000507379.6:p.His1036GlnfsTer2
	ENST00000508376.6:c.3162delC	ENST00000508376.6:p.His1054GlnfsTer2
	ENST00000509732.6:c.3162delC	ENST00000509732.6:p.His1054GlnfsTer2
	ENST00000512211.7:c.3162delC	ENST00000512211.7:p.His1054GlnfsTer2
	ENST00000713638.1:c.*1144delC
	ENST00000713639.1:c.2844delC	ENST00000713639.1:p.His948GlnfsTer2

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	2013-11-14	criteria provided, single submitter	Familial multiple polyposis syndrome	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.777	Adenomatous Polyposis Coli	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000038.6(APC):c.3162del (p.His1054fs) AND Familial multiple polyposis syndrome	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: rs397515733 dbSNP
Genome: hg38
Position: chr5:112,838,756-112,838,756
Variant Type: snv
Reference Allele: C
Alternative Allele: -

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