RGD:150450025 Rat Genome Database

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Variant: RGD:150450025 -  Homo sapiens

RGD ID: 150450025
RS ID: rs12667262
ClinVar ID: CV1215189
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMPER  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 34,006,362
GRCh38 7 33,966,750
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1276:g.66840G>A
NG_031933.1:g.66840G>A
NC_000007.14:g.33966750G>A
NC_000007.13:g.34006362G>A
More... 		11/10/2018 intron variant benign none provided

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

Gene Symbol:BMPER
Accession:XM_047419939
Location:INTRON

Gene Symbol:BMPER
Accession:NM_001365308
Location:INTRON

Gene Symbol:BMPER
Accession:NM_133468
Location:INTRON

Gene Symbol:BMPER
Accession:NM_001410872
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001611779 CLINVAR
dbSNP (RS) rs12667262 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMPER CLINVAR
OMIM 608699 CLINVAR