rs112266944 Rat Genome Database

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Variant: rs112266944 -  Homo sapiens

RGD ID: 14723408
RS ID: rs112266944
ClinVar ID: CV658744
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC19A3  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 228,563,270
GRCh38 2 227,698,554
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.979+182A>G
NG_016359.1:g.24476A>G
NC_000002.12:g.227698554T>C
NC_000002.11:g.228563270T>C
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC19A3
Accession:NM_001371411
Location:INTRON

Gene Symbol:SLC19A3
Accession:XM_047445927
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_025243
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371413
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371412
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371414
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832521 CLINVAR
dbSNP (RS) rs112266944 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC19A3 CLINVAR
OMIM 606152 CLINVAR