Variant #0000283731 (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 likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48026630C>G
DNA change (hg38) g.47799491C>G
Published as MSH6(NM_000179.2):c.1508C>G (p.S503C, p.(Ser503Cys)), MSH6(NM_000179.3):c.1508C>G (p.S503C)
ISCN -
DB-ID MSH6_000149 See all 33 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00063 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -?/. - c.1508C>G r.(?) p.(Ser503Cys)
FBXO11 NM_001190274.1 -?/. - c.*8627G>C r.(=) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.