Variant #0000605193 (NC_000001.10:g.220324706T>C, NM_012414.3:c.4069A>G (RAB3GAP2))

Chromosome 1
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.220324706T>C
DNA change (hg38) g.220151364T>C
Published as RAB3GAP2(NM_012414.4):c.4069A>G (p.T1357A)
ISCN -
DB-ID RAB3GAP2_000064
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB3GAP2 NM_012414.3 ?/. - c.4069A>G r.(?) p.(Thr1357Ala)
IARS2 NM_018060.3 ?/. - c.*3729T>C r.(=) p.(=)


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