Variant #0000251736 (NC_000021.8:g.35742799A>G, NM_172201.1:c.22A>G (KCNE2))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35742799A>G
DNA change (hg38) g.34370500A>G
Published as KCNE2(NM_172201.1):c.22A>G (p.T8A), KCNE2(NM_172201.2):c.22A>G (p.T8A)
ISCN -
DB-ID KCNE2_000032 See all 6 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) 0.00372 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNE2 NM_172201.1 -?/. - c.22A>G r.(?) p.(Thr8Ala)


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