Variant #0000568268 (NC_000019.9:g.51165832dup, NM_016148.2:c.5879dup (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.51165832dup
DNA change (hg38) g.50662575dup
Published as SHANK1(NM_016148.2):c.5879dupC (p.(Thr1961TyrfsTer74))
ISCN -
DB-ID C19orf81_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 11:15:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf81 NM_001195076.1 ?/. - c.*3433dup r.(?) p.(=)
SHANK1 NM_016148.2 ?/. - c.5879dup r.(?) p.(Thr1961TyrfsTer74)


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