RGD:15106742 Rat Genome Database

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Variant: RGD:15106742 -  Homo sapiens

RGD ID: 15106742
RS ID: rs142331784
ClinVar ID: CV779100
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRLR  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 35,070,219
GRCh38 5 35,070,117
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001204318.1:c.685+7G>A
NM_001204314.2:c.382+7G>A
NM_000949.7:c.685+7G>A
NM_001204315.1:c.685+7G>A
More... 		06/27/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRLR
Accession:XM_011514068
Location:INTRON

Gene Symbol:PRLR
Accession:XM_047417390
Location:INTRON

Gene Symbol:PRLR
Accession:NM_001204317
Location:INTRON

Gene Symbol:PRLR
Accession:NM_001204315
Location:INTRON

Gene Symbol:PRLR
Accession:NM_001204318
Location:INTRON

Gene Symbol:PRLR
Accession:XM_047417388
Location:INTRON

Gene Symbol:PRLR
Accession:NM_001204314
Location:INTRON

Gene Symbol:PRLR
Accession:XM_006714484
Location:INTRON

Gene Symbol:PRLR
Accession:XM_047417391
Location:INTRON

Gene Symbol:PRLR
Accession:NM_001204316
Location:INTRON

Gene Symbol:PRLR
Accession:NM_000949
Location:INTRON

Gene Symbol:PRLR
Accession:XM_024446131
Location:INTRON

Gene Symbol:PRLR
Accession:NR_037910
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000960143 CLINVAR
dbSNP (RS) rs142331784 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRLR CLINVAR
OMIM 176761 CLINVAR