Variant #0000887735 (NC_000007.13:g.150655331del, NM_000238.3:c.732del (KCNH2))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.150655331del
DNA change (hg38) -
Published as KCNH2(NM_000238.4):c.732delG (p.G246Afs*114)
ISCN -
DB-ID KCNH2_001367
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +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.732del r.(?) p.(Gly246Alafs*114)
KCNH2 NM_172057.2 +/. - c.-2740del r.(?) p.(=)


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