RGD:14745768 Rat Genome Database

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Variant: RGD:14745768 -  Homo sapiens

RGD ID: 14745768
RS ID: rs655928
ClinVar ID: CV666203
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNE3  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 74,168,982
GRCh38 11 74,457,937
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005472.5:c.-40-334A>G
NG_011833.1:g.14619A>G
NC_000011.10:g.74457937T>C
NC_000011.9:g.74168982T>C
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KCNE3
Accession:XM_047426177
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:XM_017017048
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:NM_005472
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:XM_047426176
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:XM_017017047
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:XM_017017051
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:XM_017017049
Location:5UTRS;INTRON

Gene Symbol:KCNE3
Accession:XM_011544713
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000843726 CLINVAR
dbSNP (RS) rs655928 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KCNE3 CLINVAR
OMIM 604433 CLINVAR