RGD:150488816 Rat Genome Database

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Variant: RGD:150488816 -  Homo sapiens

RGD ID: 150488816
RS ID: rs7665167
ClinVar ID: CV1237540
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMPR1B  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 96,025,302
GRCh38 4 95,104,151
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001203.3:c.-17-257T>G
NM_001256792.2:c.-17-257T>G
NM_001256794.1:c.-17-257T>G
NM_001256793.2:c.74-257T>G
More... 		09/04/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BMPR1B
Accession:NM_001256792
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_011532201
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_047416093
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_017008558
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:NM_001256794
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_017008560
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_047416091
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_047416095
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:NM_001203
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_017008559
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:XM_047416094
Location:5UTRS;INTRON

Gene Symbol:BMPR1B
Accession:NM_001256793
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001654389 CLINVAR
dbSNP (RS) rs7665167 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMPR1B CLINVAR
OMIM 603248 CLINVAR