Variant #0000290058 (NC_000001.10:g.160011280C>T, NM_002241.4:c.1043G>A (KCNJ10))

Chromosome 1
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.160011280C>T
DNA change (hg38) g.160041490C>T
Published as KCNJ10(NM_002241.4):c.1043G>A (p.R348H), KCNJ10(NM_002241.5):c.1043G>A (p.(Arg348His))
ISCN -
DB-ID KCNJ10_000004 See all 4 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) 0.0004 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNJ10 NM_002241.4 ?/. - c.1043G>A r.(?) p.(Arg348His)


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