Variant #0001033395 (NC_000002.11:g.48132711_48132713del, NM_000179.2:c.*98712_*98714del (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48132711_48132713del
DNA change (hg38) -
Published as FBXO11(NM_001190274.2):c.167_169del (p.(Gln56del)), FBXO11(NM_001190274.2):c.167_169delAGC (p.Q56del)
ISCN -
DB-ID MSH6_001290 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.*98712_*98714del r.(=) p.(=)
FBXO11 NM_001190274.1 -?/. - c.167_169del r.(?) p.(Gln56del)


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