Variant #0001065171 (NC_000009.11:g.139272464_139272469dup, NM_003086.2:c.3814_3819dup (SNAPC4))

Chromosome 9
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.139272464_139272469dup
DNA change (hg38) -
Published as SNAPC4(NM_003086.3):c.3814_3819dup (p.(Gly1272_Leu1273dup))
ISCN -
DB-ID chr9_008601
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNAPC4 NM_003086.2 ?/. - c.3814_3819dup r.(?) p.(Gly1272_Leu1273dup)
CARD9 NM_052813.4 ?/. - c.-4498_-4493dup r.(?) p.(=)


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