Variant #0000516365 (NC_000002.11:g.48033390_48033392del, NM_000179.2:c.3694_3696del (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48033390_48033392del
DNA change (hg38) g.47806251_47806253del
Published as MSH6(NM_000179.3):c.3694_3696delGTT (p.V1232del)
ISCN -
DB-ID MSH6_000721 See all 5 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +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.3694_3696del r.(?) p.(Val1232del)
FBXO11 NM_001190274.1 +?/. - c.*1868_*1870del r.(=) p.(=)


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