Variant #0000509254 (NC_000002.11:g.135887600C>T, NM_001172435.1:c.1009C>T (RAB3GAP1))

Chromosome 2
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.135887600C>T
DNA change (hg38) g.135130030C>T
Published as -
ISCN -
DB-ID RAB3GAP1_000037 See all 4 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
RAB3GAP1 NM_001172435.1 +/. - c.1009C>T r.(?) p.(Arg337Ter)
RAB3GAP1 NM_012233.2 +/. - c.1009C>T r.(?) p.(Arg337Ter)


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