Variant #0000278366 (NC_000011.9:g.128781442G>A, NM_000890.3:c.274G>A (KCNJ5))

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.128781442G>A
DNA change (hg38) g.128911547G>A
Published as KCNJ5(NM_000890.5):c.274G>A (p.V92I)
ISCN -
DB-ID KCNJ5_000013
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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
KCNJ5 NM_000890.3 ?/. - c.274G>A r.(?) p.(Val92Ile)
C11orf45 NM_145013.2 ?/. - c.-6044C>T r.(?) p.(=)


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