Variant #0000538511 (NC_000009.11:g.79867230_79867233del, NM_033305.2:c.2250_2253del (VPS13A))

Chromosome 9
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.79867230_79867233del
DNA change (hg38) g.77252314_77252317del
Published as VPS13A(NM_033305.2):c.2250_2253delGTCT (p.S751Rfs*8)
ISCN -
DB-ID VPS13A_000172
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13A NM_033305.2 +/. - c.2250_2253del r.(?) p.(Ser751ArgfsTer8)


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