Variant #0001050803 (NC_000002.11:g.135911323del, NM_001172435.1:c.2166del (RAB3GAP1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.135911323del
DNA change (hg38) -
Published as RAB3GAP1(NM_012233.3):c.2166del (p.(Gly723Glufs*3))
ISCN -
DB-ID RAB3GAP1_000105
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB3GAP1 NM_001172435.1 +?/. - c.2166del r.(?) p.(Gly723Glufs*3)
RAB3GAP1 NM_012233.2 +?/. - c.2166del r.(?) p.(Gly723Glufs*3)


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