chr2:47476408:G>T Detail (hg38) (MSH2)

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

Genome

Assembly	Position
hg19	chr2:47,703,547-47,703,547 View the variant detail on this assembly version.
hg38	chr2:47,476,408-47,476,408

HGVS

MSH2

Type	Transcript	Protein
RefSeq	NM_000251.2:c.2047G>T	NP_000242.1:p.Gly683Trp
	NM_001258281.1:c.1849G>T	NP_001245210.1:p.Gly617Trp
Ensemble	ENST00000233146.7:c.2047G>T	ENST00000233146.7:p.Gly683Trp
	ENST00000406134.5:c.2047G>T	ENST00000406134.5:p.Gly683Trp
	ENST00000543555.6:c.1849G>T	ENST00000543555.6:p.Gly617Trp
	ENST00000645506.1:c.2047G>T	ENST00000645506.1:p.Gly683Trp
	ENST00000713854.1:c.1897G>T	ENST00000713854.1:p.Gly633Trp
	ENST00000713919.1:c.1768G>T	ENST00000713919.1:p.Gly590Trp

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

MSH2

Type	Database	ID	Link
Gene	MIM	609309	OMIM
	HGNC	7325	HGNC
	Ensembl	ENSG00000095002	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM6972301	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.332	Hereditary Nonpolyposis Colorectal Cancer	NA	CLINVAR		Detail
0.121	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
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: rs267607995 dbSNP
Genome: hg38
Position: chr2:47,476,408-47,476,408
Variant Type: snv
Reference Allele: G
Alternative Allele: T

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