Variant #0000889697 (NC_000011.9:g.128786323G>A, NM_000890.3:c.957G>A (KCNJ5))

Chromosome 11
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.128786323G>A
DNA change (hg38) -
Published as KCNJ5(NM_000890.3):c.957G>A (p.R319=), KCNJ5(NM_001354169.2):c.957G>A (p.R319=)
ISCN -
DB-ID C11orf45_000019 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) 0.00105 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNJ5 NM_000890.3 -/. - c.957G>A r.(?) p.(Arg319=)
C11orf45 NM_145013.2 -/. - c.-10925C>T r.(?) p.(=)


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