Variant #0000866927 (NC_000022.10:g.51160126_51160133del, NM_033517.1:c.3826_3833del (SHANK3))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51160126_51160133del
DNA change (hg38) -
Published as SHANK3(NM_033517.1):c.3827_3834del (p.(Gln1289Valfs*4))
ISCN -
DB-ID SHANK3_000238 See all 2 reported entries
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHANK3 NM_001372044.1 +?/. - c.4090_4097del r.(?) p.(Gln1364Valfs*4)
SHANK3 NM_033517.1 +?/. - c.3826_3833del r.(?) p.(Gln1276Valfs*4)


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