Variant #0000538501 (NC_000009.11:g.79834890A>G, NM_033305.2:c.775A>G (VPS13A))

Chromosome 9
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.79834890A>G
DNA change (hg38) g.77219974A>G
Published as VPS13A(NM_033305.2):c.775A>G (p.N259D), VPS13A(NM_033305.3):c.775A>G (p.N259D)
ISCN -
DB-ID VPS13A_000076 See all 3 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) 0.00242 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
VPS13A NM_033305.2 -?/. - c.775A>G r.(?) p.(Asn259Asp)


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