chr5:112779849:G>A 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	chr5:112,115,546-112,115,546 View the variant detail on this assembly version.
hg38	chr5:112,779,849-112,779,849

HGVS

APC

Type	Transcript	Protein
RefSeq	NM_000038.5:c.532-941G>A
	NM_001127511.2:c.562-941G>A
	NM_001127510.2:c.532-941G>A
Ensemble	ENST00000257430.9:c.532-941G>A
	ENST00000504915.3:c.532-941G>A
	ENST00000507379.6:c.562-941G>A
	ENST00000508376.6:c.532-941G>A
	ENST00000509732.6:c.532-941G>A
	ENST00000512211.7:c.532-941G>A
	ENST00000713638.1:c.532-941G>A
	ENST00000713639.1:c.355-941G>A

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

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

[No Data.]

CIViC

[No Data.]

DisGeNET

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

Annotation

Annotations

Descrption	Source	Links
NA	DisGeNET	Detail

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs730881227 dbSNP
Genome: hg38
Position: chr5:112,779,849-112,779,849
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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