Variant #0001003244 (NC_000017.10:g.40854581A>G, NM_003632.2:c.*3653A>G (CNTNAP1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40854581A>G
DNA change (hg38) -
Published as EZH1(NM_001991.3):c.2213T>C (p.(Leu738Pro))
ISCN -
DB-ID CNTNAP1_000017
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EZH1 NM_001991.3 ?/. - c.2213T>C r.(?) p.(Val738Ala)
CNTNAP1 NM_003632.2 ?/. - c.*3653A>G r.(=) p.(=)


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