RGD:15103305 Rat Genome Database

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Variant: RGD:15103305 -  Homo sapiens

RGD ID: 15103305
RS ID: rs115890291
ClinVar ID: CV730560
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC39A14  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 22,275,155
GRCh38 8 22,417,642
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001128431.4:c.1148-9C>T
NM_001135153.3:c.1148-9C>T
NM_001135154.3:c.1148-9C>T
NM_001351655.2:c.1148-9C>T
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC39A14
Accession:NM_015359
Location:INTRON

Gene Symbol:SLC39A14
Accession:XM_047421653
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001351656
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001351659
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001351658
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001351660
Location:INTRON

Gene Symbol:SLC39A14
Accession:XM_047421655
Location:INTRON

Gene Symbol:SLC39A14
Accession:XM_006716324
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001128431
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001351657
Location:INTRON

Gene Symbol:SLC39A14
Accession:XM_047421654
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001135154
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001135153
Location:INTRON

Gene Symbol:SLC39A14
Accession:NM_001351655
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000892645 CLINVAR
dbSNP (RS) rs115890291 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC39A14 CLINVAR
OMIM 608736 CLINVAR