Variant #0000866921 (NC_000022.10:g.51123008C>T, NC_000022.10(NM_033517.1):c.964-5C>T (SHANK3))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.51123008C>T
DNA change (hg38) -
Published as SHANK3(NM_033517.1):c.964-5C>T (p.?)
ISCN -
DB-ID SHANK3_000229
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) 0.00104 View details
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.1189-5C>T r.spl? p.?
SHANK3 NM_033517.1 -?/. - c.964-5C>T r.spl? p.?


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