RGD:150507513 Rat Genome Database

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Variant: RGD:150507513 -  Homo sapiens

RGD ID: 150507513
RS ID: rs3024458
ClinVar ID: CV1211194
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: F13A1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 6,151,952
GRCh38 6 6,151,719
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000129.4:c.2045+94G>A
LRG_549:g.173973G>A
NG_008107.1:g.173973G>A
NC_000006.12:g.6151719C>T
More... 		11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:F13A1
Accession:NM_000129
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001596313 CLINVAR
dbSNP (RS) rs3024458 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene F13A1 CLINVAR
OMIM 134570 CLINVAR