RGD:11662944 Rat Genome Database

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Variant: RGD:11662944 -  Homo sapiens

RGD ID: 11662944
RS ID: rs886061659
ClinVar ID: CV308382
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: F13A1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 6,145,810
GRCh38 6 6,145,577
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
LRG_549t1:c.*42G>A
LRG_549:g.180115G>A
NG_008107.1:g.180115G>A
NC_000006.12:g.6145577C>T
More... 		01/13/2018 3 prime utr variant uncertain significance all ages <1 / 1 000 000 Factor XIII subunit A deficiency
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:F13A1
Accession:NM_000129
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000390945 CLINVAR
dbSNP (RS) rs886061659 CLINVAR
MedGen C2750514 CLINVAR
NCBI Gene F13A1 CLINVAR
OMIM 134570 CLINVAR
  613225 CLINVAR