Variant #0000721789 (NC_000008.10:g.133492610A>G, NM_004519.3:c.170T>C (KCNQ3))

Chromosome 8
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.133492610A>G
DNA change (hg38) -
Published as KCNQ3(NM_004519.3):c.170T>C (p.(Leu57Pro)), KCNQ3(NM_004519.4):c.170T>C (p.L57P)
ISCN -
DB-ID KCNQ3_000069 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.170T>C r.(?) p.(Leu57Pro)


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