RGD:150487523 Rat Genome Database

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Variant: RGD:150487523 -  Homo sapiens

RGD ID: 150487523
RS ID: rs76432597
ClinVar ID: CV1262754
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SERPINI1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 167,542,069
GRCh38 3 167,824,281
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001122752.2:c.1067-192G>A
NM_005025.5:c.1067-192G>A
NG_008217.1:g.93638G>A
NC_000003.12:g.167824281G>A
More... 		05/25/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SERPINI1
Accession:NM_005025
Location:INTRON

Gene Symbol:SERPINI1
Accession:NM_001122752
Location:INTRON

Gene Symbol:SERPINI1
Accession:XM_017006618
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001687152 CLINVAR
dbSNP (RS) rs76432597 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SERPINI1 CLINVAR
OMIM 602445 CLINVAR