Variant #0001035888 (NC_000006.11:g.73839568C>T, NC_000006.11(NM_019842.3):c.1248-3576C>T (KCNQ5))

Chromosome 6
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.73839568C>T
DNA change (hg38) -
Published as KCNQ5(NM_001160132.2):c.1273C>T (p.(Gln425*))
ISCN -
DB-ID KCNQ5_000053
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 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 2025-05-05 21:14:00 +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     
KCNQ5 NM_019842.3 ?/. - c.1248-3576C>T r.(=) p.(=)


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