Variant #0000991622 (NC_000002.11:g.135887597C>T, NM_001172435.1:c.1006C>T (RAB3GAP1))

Chromosome 2
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.135887597C>T
DNA change (hg38) -
Published as RAB3GAP1(NM_001172435.1):c.1006C>T (p.R336C), RAB3GAP1(NM_012233.2):c.1006C>T (p.(Arg336Cys))
ISCN -
DB-ID RAB3GAP1_000020 See all 2 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) 0.00434 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +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.1006C>T r.(?) p.(Arg336Cys)
RAB3GAP1 NM_012233.2 -?/. - c.1006C>T r.(?) p.(Arg336Cys)


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