Variant #0000278341 (NC_000007.13:g.150671805T>G, NM_000238.3:c.301A>C (KCNH2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.150671805T>G
DNA change (hg38) g.150974717T>G
Published as KCNH2(NM_000238.4):c.301A>C (p.K101Q)
ISCN -
DB-ID KCNH2_001201
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 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.301A>C r.(?) p.(Lys101Gln)
KCNH2 NM_172057.2 +?/. - c.-19214A>C r.(?) p.(=)


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