RGD:150336548 Rat Genome Database

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Variant: RGD:150336548 -  Homo sapiens

RGD ID: 150336548
RS ID: rs6487521
ClinVar ID: CV1172482
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C1R  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 7,243,040
GRCh38 12 7,090,444
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1321t1:c.232-196G>A
LRG_1321:g.7164G>A
NG_062465.1:g.7164G>A
NC_000012.11:g.7243040C>T
More... 		05/10/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:C1R
Accession:NM_001733
Location:INTRON

Gene Symbol:C1R
Accession:NM_001354346
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001541039 CLINVAR
dbSNP (RS) rs6487521 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C1R CLINVAR
OMIM 613785 CLINVAR