Variant #0000417749 (NC_000002.11:g.48033977T>A, NM_000179.2:c.4061T>A (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.48033977T>A
DNA change (hg38) g.47806838T>A
Published as L1354Q
ISCN -
DB-ID MSH6_000306 See all 6 reported entries
Variant remarks pull down assay interaction with MSH2-WT and MSH2-I145M is comparable to MSH6-WT
Reference PubMed: Kariola 2003
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rolf Sijmons
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2009-04-24 17:16:00 +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     
MSH6 NM_000179.2 ?/. 10 c.4061T>A r.(?) p.(Leu1354Gln)


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