Variant #0001013765 (NC_000002.11:g.48030647dup, NM_000179.2:c.3261dup (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.48030647dup
DNA change (hg38) -
Published as MSH6(NM_000179.2):c.3261dup (p.(Phe1088Leufs*5)), MSH6(NM_000179.2):c.3261dupC (p.F1088Lfs*5), MSH6(NM_000179.2):c.3261dupC (p.Phe1088Leufs*5), MSH...
ISCN -
DB-ID MSH6_000077 See all 48 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 20:49:11 +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.3261dup r.(?) p.(Phe1088LeufsTer5)
FBXO11 NM_001190274.1 +/. - c.*4617dup r.(?) p.(=)


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