Variant #0000538288 (NC_000009.11:g.43915405G>A, NM_001201380.1:c.3488G>A (CNTNAP3B))

Chromosome 9
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.43915405G>A
DNA change (hg38) -
Published as CNTNAP3B(NM_001201380.1):c.3488G>A (p.(Gly1163Asp))
ISCN -
DB-ID CNTNAP3B_000011
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNTNAP3B NM_001201380.1 -?/. - c.3488G>A r.(?) p.(Gly1163Asp)


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