Variant #0000531110 (NC_000007.13:g.145814041G>A, NM_014141.5:c.73G>A (CNTNAP2))

Chromosome 7
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.145814041G>A
DNA change (hg38) g.146116949G>A
Published as CNTNAP2(NM_014141.5):c.73G>A (p.A25T, p.(Ala25Thr)), CNTNAP2(NM_014141.6):c.73G>A (p.A25T)
ISCN -
DB-ID CNTNAP2_000101 See all 4 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) 0.0011 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 2019-07-18 18:22:55 +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     
CNTNAP2 NM_014141.5 ?/. - c.73G>A r.(?) p.(Ala25Thr)


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