Variant #0000982505 (NC_000017.10:g.40850632T>C, NC_000017.10(NM_003632.2):c.3863-4T>C (CNTNAP1))

Chromosome 17
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.40850632T>C
DNA change (hg38) -
Published as CNTNAP1(NM_003632.3):c.3863-4T>C
ISCN -
DB-ID CNTNAP1_000014
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EZH1 NM_001991.3 -?/. - c.*3918A>G r.(=) p.(=)
CNTNAP1 NM_003632.2 -?/. - c.3863-4T>C r.spl? p.?


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