Variant #0000009589 (NC_000002.11:-, MSH6(NM_000179.2):c.3488A>T)

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type c.3488A>T
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MSH6_00005
Frequency 0.0256
Variant remarks Substitution
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 ./. 06 c.3488A>T - p.Glu1163Val