Variant #0001047985 (NC_000011.9:g.128786440C>A, NM_000890.3:c.1074C>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.128786440C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID KCNJ5_000027
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2136003967
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-12 15:34:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNJ5 NM_000890.3 ?/. - c.1074C>A r.(?) p.(Asn358Lys)


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