Variant #0000862883 (NC_000012.11:g.122710546T>G, NM_019887.5:c.16A>C (DIABLO))

Chromosome 12
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.122710546T>G
DNA change (hg38) -
Published as DIABLO(NM_019887.5):c.16A>C (p.S6R)
ISCN -
DB-ID VPS33A_000005
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIABLO NM_001371333.1 -?/. - c.16A>C r.(?) p.(Ser6Arg)
DIABLO NM_019887.5 -?/. - c.16A>C r.(?) p.(Ser6Arg)
VPS33A NM_022916.4 -?/. - c.*6247A>C r.(=) p.(=)


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