Variant #0000417714 (NC_000002.11:g.48026630C>G, NM_000179.2:c.1508C>G (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.48026630C>G
DNA change (hg38) g.47799491C>G
Published as S503C
ISCN -
DB-ID MSH6_000149 See all 33 reported entries
Variant remarks ClustalW AA not conserved
Reference PubMed: Barnetson 2008
ClinVar ID -
dbSNP ID -
Origin In silico
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00063 View details
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 22:02:15 +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 -?/. 4 c.1508C>G r.(?) p.(Ser503Cys)


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