Variant #0000282612 (NC_000002.11:g.48026312_48026313del, NM_000179.2:c.1190_1191del (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.48026312_48026313del
DNA change (hg38) g.47799173_47799174del
Published as MSH6(NM_000179.3):c.1190_1191delAT (p.Y397Cfs*3)
ISCN -
DB-ID MSH6_000382 See all 7 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 2018-01-15 20:58:59 +01:00 (CET)
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.1190_1191del r.(?) p.(Tyr397CysfsTer3)
FBXO11 NM_001190274.1 +/. - c.*8945_*8946del r.(=) p.(=)


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