Variant #0000516587 (NC_000002.11:g.65331874C>A, NM_004161.4:c.90G>T (RAB1A))

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.65331874C>A
DNA change (hg38) g.65104740C>A
Published as RAB1A(NM_004161.5):c.90G>T (p.R30S)
ISCN -
DB-ID RAB1A_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-10 19:18:43 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB1A NM_004161.4 ?/. - c.90G>T r.(?) p.(Arg30Ser)
CEP68 NM_015147.2 ?/. - c.*21106C>A r.(=) p.(=)


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