RGD:34898681 Rat Genome Database

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Variant: RGD:34898681 -  Homo sapiens

RGD ID: 34898681
RS ID: rs775468885
ClinVar ID: CV915477
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMPR1A  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 88,678,924
GRCh38 10 86,919,167
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_298t1:c.869-5G>T
NM_004329.3:c.869-5G>T
LRG_298:g.167529G>T
NG_009362.1:g.167529G>T
More... 		04/17/2019 intron variant uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:BMPR1A
Accession:NM_001406580
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406581
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406572
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406571
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_004329
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406563
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406570
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406561
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406562
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406569
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406568
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406575
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406565
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406578
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406588
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406560
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406582
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406577
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406573
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406576
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406584
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406579
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406564
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406574
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406583
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406589
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406587
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406585
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406567
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406566
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406559
Location:INTRON

Gene Symbol:BMPR1A
Accession:NM_001406586
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:BMPR1A
Accession:XM_047425680
Location:INTRON

Gene Symbol:BMPR1A
Accession:NR_176212
Location:INTRON;NON-CODING

Gene Symbol:BMPR1A
Accession:NR_176213
Location:INTRON;NON-CODING

Gene Symbol:BMPR1A
Accession:NR_176211
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001180185 CLINVAR
dbSNP (RS) rs775468885 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene BMPR1A CLINVAR
OMIM 601299 CLINVAR
SNOMED CT 699346009 CLINVAR