Variant #0000992931 (NC_000002.11:g.48132720_48132743dup, NM_000179.2:c.*98721_*98744dup (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48132720_48132743dup
DNA change (hg38) -
Published as FBXO11(NM_001190274.1):c.123_146dupCCAGCAGCAGCCTCCGCCGCCGCC (p.(Pro49_Gln50insGlnGlnGlnProProProProPro))
ISCN -
DB-ID MSH6_011143
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.*98721_*98744dup r.(=) p.(=)
FBXO11 NM_001190274.1 ?/. - c.123_146dup r.(?) p.(Pro45_Gln52dup)


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