Variant #0000321947 (NC_000011.9:g.2683246C>A, NM_000218.2:c.1449C>A (KCNQ1))

Chromosome 11
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.2683246C>A
DNA change (hg38) g.2662016C>A
Published as KCNQ1(NM_000218.2):c.1449C>A (p.(Asn483Lys)), KCNQ1(NM_000218.3):c.1449C>A (p.N483K), KCNQ1OT1(NR_002728.3):n.37983G>T
ISCN -
DB-ID KCNQ1OT1_000002 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_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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNQ1 NM_000218.2 ?/. - c.1449C>A r.(?) p.(Asn483Lys)
KCNQ1OT1 NR_002728.2 ?/. - n.37983G>T r.(?) -


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