RGD:150500992 Rat Genome Database

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Variant: RGD:150500992 -  Homo sapiens

RGD ID: 150500992
RS ID: rs73804338
ClinVar ID: CV1223609
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC34A1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 176,812,908
GRCh38 5 177,385,907
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001167579.2:c.109+57A>G
NM_003052.5:c.109+57A>G
NG_016223.1:g.6477A>G
NC_000005.10:g.177385907A>G
More... 		11/10/2018 intron variant benign none provided

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

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SLC34A1
Accession:NM_001167579
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SLC34A1
Accession:NM_003052
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001620730 CLINVAR
dbSNP (RS) rs73804338 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC34A1 CLINVAR
OMIM 182309 CLINVAR