RGD:28893322 Rat Genome Database

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Variant: RGD:28893322 -  Homo sapiens

RGD ID: 28893322
RS ID: rs1038526436
ClinVar ID: CV892560
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMPR1B  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 96,076,889
GRCh38 4 95,155,738
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001256792.2:c.*1065T>A
NC_000004.12:g.95155738T>A
NC_000004.11:g.96076889T>A
NM_001203.2:c.*1065T>A
More... 		01/13/2018 3 prime utr variant uncertain significance Brachydactyly (disease); Brachydactyly syndrome
Disease Annotations     Click to see Annotation Detail View
brachydactyly  (IAGP)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Brachydactyly  (IAGP)

Variant Details
Variant Transcripts
Gene Symbol:BMPR1B
Accession:XM_011532201
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_017008559
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_017008560
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:NM_001256793
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:NM_001203
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_047416093
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_047416095
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:NM_001256794
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_047416091
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:NM_001256792
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_017008558
Location:3UTRS;EXON

Gene Symbol:BMPR1B
Accession:XM_047416094
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001153494 CLINVAR
dbSNP (RS) rs1038526436 CLINVAR
MedGen C0221357 CLINVAR
NCBI Gene BMPR1B CLINVAR
OMIM 603248 CLINVAR
SNOMED CT 43476002 CLINVAR