RGD:15195185 Rat Genome Database

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Variant: RGD:15195185 -  Homo sapiens

RGD ID: 15195185
RS ID: rs17221987
ClinVar ID: CV730109
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC11A1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 219,257,697
GRCh38 2 218,392,974
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000578.4:c.1165-7A>C
NG_012128.1:g.15946A>C
NC_000002.12:g.218392974A>C
NC_000002.11:g.219257697A>C
More... 		08/22/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC11A1
Accession:XM_047445573
Location:INTRON

Gene Symbol:SLC11A1
Accession:XM_005246793
Location:INTRON

Gene Symbol:SLC11A1
Accession:XM_047445575
Location:INTRON

Gene Symbol:SLC11A1
Accession:XM_047445574
Location:INTRON

Gene Symbol:SLC11A1
Accession:XM_017004766
Location:INTRON

Gene Symbol:SLC11A1
Accession:NM_000578
Location:INTRON

Gene Symbol:SLC11A1
Accession:XM_006712711
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000889432 CLINVAR
dbSNP (RS) rs17221987 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC11A1 CLINVAR
OMIM 600266 CLINVAR