RGD:11666721 Rat Genome Database

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Variant: RGD:11666721 -  Homo sapiens

RGD ID: 11666721
ClinVar ID: CV315145
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNE3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 74,166,543
GRCh38 11 74,455,498
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_439t1:c.*1754A>T
NM_005472.4:c.*1754A>T
LRG_439:g.17058A>T
NG_011833.1:g.17058A>T
More... 		06/14/2016 3 prime utr variant likely benign Sudden unexpected nocturnal death syndrome; Sudden Unexplained Death Syndrome; Sudden unexplained nocturnal death syndrome; Sudden Unexplained Nocturnal Death Syndrome (SUNDS)

Variant Details
Variant Transcripts
Gene Symbol:KCNE3
Accession:NM_005472
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_017017049
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_017017048
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_047426176
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_011544713
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_017017047
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_017017051
Location:3UTRS;EXON

Gene Symbol:KCNE3
Accession:XM_047426177
Location:3UTRS;EXON

Variant Samples