RGD:150455392 Rat Genome Database

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Variant: RGD:150455392 -  Homo sapiens

RGD ID: 150455392
RS ID: rs2274391
ClinVar ID: CV1220453
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: F13A1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 6,195,926
GRCh38 6 6,195,693
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_549:g.129999G>A
NG_008107.1:g.129999G>A
NM_000129.4:c.1305+104G>A
NC_000006.12:g.6195693C>T
More... 		06/19/2021 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 RCV001612546 CLINVAR
dbSNP (RS) rs2274391 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene F13A1 CLINVAR
OMIM 134570 CLINVAR