Variant #0000324926 (NC_000016.9:g.76587220G>A, NM_033401.3:c.3483G>A (CNTNAP4))

Chromosome 16
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.76587220G>A
DNA change (hg38) g.76553323G>A
Published as CNTNAP4(NM_001322189.1):c.3219G>A (p.W1073*), CNTNAP4(NM_033401.3):c.3482G>A (p.(Arg1161His))
ISCN -
DB-ID CNTNAP4_000013 See all 2 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) 0.00025 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNTNAP4 NM_033401.3 ?/. - c.3483G>A r.(?) p.(Ala1161=)


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