Variant #0000800710 (NC_000002.11:g.48018314T>A, NC_000002.11(NM_000179.2):c.457+52T>A (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48018314T>A
DNA change (hg38) -
Published as MSH6(NM_000179.2):c.457+52T>A
ISCN -
DB-ID MSH6_000032 See all 44 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) Retrieve
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -/. - c.457+52T>A r.(=) p.(=)
FBXO11 NM_001190274.1 -/. - c.*16943A>T r.(=) p.(=)


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