chr2:47707878:TAATTTC> Detail (hg19) (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	chr2:47,707,878-47,707,884
hg38	chr2:47,480,739-47,480,745

HGVS

MSH2

Type	Transcript	Protein
RefSeq	NM_000251.2:c.2502_2508delTAATTTC	NP_000242.1:p.Asn835LeufsTer4
	NM_001258281.1:c.2304_2310delTAATTTC	NP_001245210.1:p.Asn769LeufsTer4
Ensemble	ENST00000233146.7:c.2502_2508delTAATTTC	ENST00000233146.7:p.Asn835LeufsTer4
	ENST00000406134.5:c.2502_2508delTAATTTC	ENST00000406134.5:p.Asn835LeufsTer4
	ENST00000543555.6:c.2304_2310delTAATTTC	ENST00000543555.6:p.Asn769LeufsTer4
	ENST00000645506.1:c.2502_2508delTAATTTC	ENST00000645506.1:p.Asn835LeufsTer4
	ENST00000713854.1:c.2352_2358delTAATTTC	ENST00000713854.1:p.Asn785LeufsTer4
	ENST00000713919.1:c.2223_2229delTAATTTC	ENST00000713919.1:p.Asn742LeufsTer4

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

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
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2013-09-05	reviewed by expert panel	Lynch syndrome	germline	Detail
Pathogenic	2022-05-10	criteria provided, multiple submitters, no conflicts	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2022-03-23	criteria provided, single submitter	not provided	germline unknown	Detail
Pathogenic	2024-01-26	criteria provided, single submitter	Hereditary nonpolyposis colorectal neoplasms	germline	Detail
Pathogenic	2022-01-20	criteria provided, single submitter	Hereditary nonpolyposis colon cancer	germline	Detail
Pathogenic	2023-08-09	criteria provided, multiple submitters, no conflicts	Lynch syndrome 1	unknown	Detail

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
NM_000251.3(MSH2):c.2502_2508del (p.Asn835fs) AND Lynch syndrome	ClinVar	Detail
NM_000251.3(MSH2):c.2502_2508del (p.Asn835fs) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000251.3(MSH2):c.2502_2508del (p.Asn835fs) AND not provided	ClinVar	Detail
NM_000251.3(MSH2):c.2502_2508del (p.Asn835fs) AND Hereditary nonpolyposis colorectal neoplasms	ClinVar	Detail
NM_000251.3(MSH2):c.2502_2508del (p.Asn835fs) AND Hereditary nonpolyposis colon cancer	ClinVar	Detail
NM_000251.3(MSH2):c.2502_2508del (p.Asn835fs) AND Lynch syndrome 1	ClinVar	Detail
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: rs63751447 dbSNP
Genome: hg19
Position: chr2:47,707,878-47,707,884
Variant Type: snv
Reference Allele: TAATTTC
Alternative Allele: -

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