RGD:150544156 Rat Genome Database

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Variant: RGD:150544156 -  Homo sapiens

RGD ID: 150544156
ClinVar ID: CV1313154
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: F12  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 176,829,461
GRCh38 5 177,402,460
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000505.4:c.1681-1G>C
LRG_145:g.12117G>C
NG_007568.1:g.12117G>C
LRG_145t1:c.1681-1G>C
More... 		03/26/2020 splice acceptor variant pathogenic none provided

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

Gene Symbol:SLC34A1
Accession:NM_001167579
Location:INTRON

Gene Symbol:F12
Accession:XM_011534462
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:SLC34A1
Accession:NM_003052
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:F12
Accession:NM_000505
Location:INTRON

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

Variant Samples