Variant #0001056776 (NC_000019.9:g.51171417_51171425dup, NM_016148.2:c.3794_3802dup (SHANK1))

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.51171417_51171425dup
DNA change (hg38) -
Published as SHANK1(NM_016148.5):c.3794_3802dup (p.(Glu1265_Gly1267dup))
ISCN -
DB-ID C19orf81_000048
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 2025-11-01 13:22:20 +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     
C19orf81 NM_001195076.1 ?/. - c.*9018_*9026dup r.(=) p.(=)
SHANK1 NM_016148.2 ?/. - c.3794_3802dup r.(?) p.(Glu1265_Gly1267dup)


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