RGD:150337551 Rat Genome Database

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Variant: RGD:150337551 -  Homo sapiens

RGD ID: 150337551
RS ID: rs150225538
ClinVar ID: CV1172481
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C1R  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 7,241,128
GRCh38 12 7,088,532
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1321t1:c.1038+78T>C
NM_001733.7:c.1038+78T>C
NM_001354346.2:c.1080+78T>C
LRG_1321:g.9076T>C
More... 		05/19/2021 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 RCV001541722 CLINVAR
dbSNP (RS) rs150225538 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C1R CLINVAR
OMIM 613785 CLINVAR