Variant #0000609961 (NC_000006.11:g.121629173_121629174del, NM_152730.4:c.642_643del (TBC1D32))

Chromosome 6
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.121629173_121629174del
DNA change (hg38) g.121308027_121308028del
Published as TBC1D32(NM_152730.5):c.642_643delCT (p.C215Rfs*11), TBC1D32(NM_152730.6):c.642_643delCT (p.C215Rfs*11)
ISCN -
DB-ID TBC1D32_000020 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D32 NM_152730.4 ?/. - c.642_643del r.(?) p.(Cys215ArgfsTer11)


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