rs111818722 Rat Genome Database

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Variant: rs111818722 -  Homo sapiens

RGD ID: 150413947
RS ID: rs111818722
ClinVar ID: CV1176119
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC19A3  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 228,564,316
GRCh38 2 227,699,600
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001371413.1:c.139-36G>T
NM_001371414.1:c.139-36G>T
NM_025243.4:c.151-36G>T
NG_016359.1:g.23430G>T
More... 		08/07/2018 intron variant likely 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_001371414
Location:INTRON

Gene Symbol:SLC19A3
Accession:XM_047445927
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371411
Location:INTRON

Gene Symbol:SLC19A3
Accession:NM_001371412
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001547953 CLINVAR
dbSNP (RS) rs111818722 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC19A3 CLINVAR
OMIM 606152 CLINVAR