chr5:112819133:T> 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	chr5:112,154,830-112,154,830
hg38	chr5:112,819,133-112,819,133

HGVS

APC

Type	Transcript	Protein
RefSeq	NM_000038.5:c.1101delT	NP_000029.2:p.Val368TyrfsTer86
	NM_001127511.2:c.1047delT	NP_001120983.2:p.Val350TyrfsTer86
	NM_001127510.2:c.1101delT	NP_001120982.1:p.Val368TyrfsTer86
Ensemble	ENST00000257430.9:c.1101delT	ENST00000257430.9:p.Val368TyrfsTer86
	ENST00000504915.3:c.1101delT	ENST00000504915.3:p.Val368TyrfsTer86
	ENST00000507379.6:c.1047delT	ENST00000507379.6:p.Val350TyrfsTer86
	ENST00000508376.6:c.1101delT	ENST00000508376.6:p.Val368TyrfsTer86
	ENST00000509732.6:c.1101delT	ENST00000509732.6:p.Val368TyrfsTer86
	ENST00000512211.7:c.1101delT	ENST00000512211.7:p.Val368TyrfsTer86
	ENST00000713638.1:c.1101delT	ENST00000713638.1:p.Val368TyrfsTer86
	ENST00000713639.1:c.783delT	ENST00000713639.1:p.Val262TyrfsTer86

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	2014-04-02	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	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.1101del (p.Val368fs) AND Hereditary cancer-predisposing 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: rs587782744 dbSNP
Genome: hg38
Position: chr5:112,819,133-112,819,133
Variant Type: snv
Reference Allele: T
Alternative Allele: -

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