Variant #0000278326 (NC_000007.13:g.150652568C>T, NC_000007.13(NM_000238.3):c.1128+1811G>A (KCNH2))

Chromosome 7
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.150652568C>T
DNA change (hg38) g.150955480C>T
Published as KCNH2(NM_172057.2):c.24G>A (p.A8=), KCNH2(NM_172057.3):c.24G>A (p.A8=)
ISCN -
DB-ID KCNH2_001209 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) 0.00012 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     
KCNH2 NM_000238.3 -/. - c.1128+1811G>A r.(=) p.(=)
KCNH2 NM_172057.2 -/. - c.24G>A r.(?) p.(Ala8=)


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