RGD:11625061 Rat Genome Database

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Variant: RGD:11625061 -  Homo sapiens

RGD ID: 11625061
ClinVar ID: CV343404
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC6A2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 55,736,674
GRCh38 16 55,702,762
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001043.3:c.*416C>A
NM_001172504.1:c.1830+828C>A
NG_016969.1:g.52133C>A
NC_000016.10:g.55702762C>A
More... 		06/14/2016 3 prime utr variant likely benign Irritable heart; Mitral valve prolapse syndrome; Neurocirculatory asthenia; Soldiers heart

Variant Details
Variant Transcripts
Gene Symbol:SLC6A2
Accession:NM_001172501
Location:3UTRS;EXON

Gene Symbol:SLC6A2
Accession:XM_011523299
Location:3UTRS;EXON

Gene Symbol:SLC6A2
Accession:XM_047434511
Location:3UTRS;EXON

Gene Symbol:SLC6A2
Accession:NM_001043
Location:3UTRS;EXON

Gene Symbol:SLC6A2
Accession:NM_001172502
Location:3UTRS;EXON

Gene Symbol:SLC6A2
Accession:XM_011523300
Location:3UTRS;EXON

Gene Symbol:SLC6A2
Accession:XM_011523295
Location:INTRON

Gene Symbol:SLC6A2
Accession:XM_006721263
Location:INTRON

Gene Symbol:SLC6A2
Accession:XM_047434513
Location:INTRON

Gene Symbol:SLC6A2
Accession:XM_047434512
Location:INTRON

Gene Symbol:SLC6A2
Accession:NM_001172504
Location:INTRON

Gene Symbol:SLC6A2
Accession:XM_047434510
Location:INTRON

Variant Samples