Variant #0000371605 (NC_000002.11:g.47630336G>T, NM_000251.2:c.6G>T (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47630336G>T
DNA change (hg38) g.47403197G>T
Published as -
ISCN -
DB-ID MSH2_001383 See all 2 reported entries
Variant remarks Insight class: 2
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2018-07-06 14:04:02 +02:00 (CEST)
Date last edited 2018-11-09 17:29:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 -?/-? 1 c.6G>T r.(?) p.(=)


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