Variant #0000417730 (NC_000002.11:g.48030647del, NM_000179.2:c.3261del (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.48030647del
DNA change (hg38) g.47803508del
Published as -
ISCN -
DB-ID MSH6_000037 See all 40 reported entries
Variant remarks Identified in Jurkat and KCL22 cell line
Reference PubMed: Hosoya 1998
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Michael Woods
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2006-05-16 12:00:00 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 +/. 5 c.3261del r.(?) p.(Phe1088Serfs*2)


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