Variant #0000800732 (NC_000002.11:g.48032098A>T, NM_000179.2:c.3488A>T (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.48032098A>T
DNA change (hg38) -
Published as MSH6(NM_000179.2):c.3488A>T (p.E1163V), MSH6(NM_000179.3):c.3488A>T (p.E1163V)
ISCN -
DB-ID MSH6_000511 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) 0.00099 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.3488A>T r.(?) p.(Glu1163Val)
FBXO11 NM_001190274.1 -/. - c.*3159T>A r.(=) p.(=)


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