Variant #0000974291 (NC_000002.11:g.135883827T>G, NC_000002.11(NM_001172435.1):c.899+8T>G (RAB3GAP1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.135883827T>G
DNA change (hg38) -
Published as RAB3GAP1(NM_012233.3):c.899+8T>G
ISCN -
DB-ID RAB3GAP1_000101
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) 0.0001 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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB3GAP1 NM_001172435.1 ?/. - c.899+8T>G r.(=) p.(=)
RAB3GAP1 NM_012233.2 ?/. - c.899+8T>G r.(=) p.(=)


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