Variant #0000618666 (NC_000022.10:g.51121773C>T, NM_033517.1:c.891C>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.51121773C>T
DNA change (hg38) g.50683345C>T
Published as SHANK3(NM_001372044.2):c.1188+651C>T, SHANK3(NM_033517.1):c.891C>T (p.S297=, p.(Ser297=))
ISCN -
DB-ID SHANK3_000134 See all 3 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) 0.00372 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHANK3 NM_033517.1 -?/. - c.891C>T r.(?) p.(=)


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