Variant #0000341673 (NC_000002.11:g.48028225C>T, NM_000179.2:c.3103C>T (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48028225C>T
DNA change (hg38) g.47801086C>T
Published as MSH6(NM_000179.2):c.3103C>T (p.R1035*, p.(Arg1035Ter)), MSH6(NM_000179.3):c.3103C>T (p.R1035*)
ISCN -
DB-ID MSH6_000057 See all 25 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 +/. - c.3103C>T r.(?) p.(Arg1035Ter)
FBXO11 NM_001190274.1 +/. - c.*7032G>A r.(=) p.(=)


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