Variant #0000326203 (NC_000019.9:g.11437478dup, NC_000019.9(NM_004283.3):c.473-1213dup (RAB3D))

Chromosome 19
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.11437478dup
DNA change (hg38) g.11326802dup
Published as RAB3D(NM_004283.3):c.473-1213_473-1212insC (p.?)
ISCN -
DB-ID RAB3D_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 12:23:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB3D NM_004283.3 ?/. - c.473-1213dup r.(=) p.(=)
TSPAN16 NM_012466.2 ?/. - c.696dup r.(?) p.(Ser233ValfsTer10)


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