Variant #0000611439 (NC_000008.10:g.133146616G>A, NM_004519.3:c.1720C>T (KCNQ3))

Chromosome 8
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.133146616G>A
DNA change (hg38) g.132134369G>A
Published as KCNQ3(NM_004519.3):c.1720C>T (p.P574S), KCNQ3(NM_004519.4):c.1720C>T (p.P574S)
ISCN -
DB-ID KCNQ3_000027 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) 0.00211 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNQ3 NM_004519.3 -?/. - c.1720C>T r.(?) p.(Pro574Ser)


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