rs73997321 Rat Genome Database

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Variant: rs73997321 -  Homo sapiens

RGD ID: 14724334
RS ID: rs73997321
ClinVar ID: CV658862
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC19A3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 228,553,070
GRCh38 2 227,688,354
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_025243.4:c.1173-47C>T
NG_016359.1:g.34676C>T
NC_000002.12:g.227688354G>A
NC_000002.11:g.228553070G>A
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC19A3
Accession:NM_025243
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371413
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371411
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371414
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371412
Location:INTRON

Gene Symbol:SLC19A3
Accession:XM_047445927
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000832937 CLINVAR
dbSNP (RS) rs73997321 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC19A3 CLINVAR
OMIM 606152 CLINVAR