Variant #0000533766 (NC_000008.10:g.133187799A>G, NM_004519.3:c.834T>C (KCNQ3))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133187799A>G
DNA change (hg38) g.132175552A>G
Published as KCNQ3(NM_004519.3):c.834T>C (p.L278=), KCNQ3(NM_004519.4):c.834T>C (p.L278=)
ISCN -
DB-ID KCNQ3_000064 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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.834T>C r.(?) p.(Leu278=)


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