Variant #0000642297 (NC_000021.8:g.35821733C>T, KCNE1(NM_000219.4):c.200G>A)

Individual ID 00285405
Chromosome 21
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35821733C>T
DNA change (hg38) g.34449435C>T
Published as -
ISCN -
DB-ID KCNE1_000080 See all 2 reported entries
Variant remarks -
Reference MORL Deafness Variation Database, PubMed: Priori 2013, PubMed: Kapplinger 2009, PubMed: Amendola 2015
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Global Variome, with Curator vacancy
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNE1 NM_000219.4 +/+ 4 c.200G>A r.(?) p.(Arg67His)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000286555 DNA ? - - KCNE1 1 Global Variome, with Curator vacancy