Variant #0000673715 (NC_000002.11:g.47630461C>T, NM_000251.2:c.131C>T (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method InSiGHT
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47630461C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MSH2_000284 See all 14 reported entries
Variant remarks Insight class: 3
Reference PubMed: Rath et al 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2020-07-07 07:16:27 +02:00 (CEST)
Date last edited 2020-07-14 21:54:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 ?/. - c.131C>T r.(?) p.(Thr44Met)


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