rs75553033 Rat Genome Database

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Variant: rs75553033 -  Homo sapiens

RGD ID: 150423456
RS ID: rs75553033
ClinVar ID: CV1183617
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RETREG1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 16,566,079
GRCh38 5 16,565,970
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001034850.3:c.428-177C>T
LRG_363:g.56040C>T
NG_016644.2:g.56040C>T
NC_000005.10:g.16565970G>A
More... 		04/22/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RETREG1
Accession:XM_011514054
Location:INTRON

Gene Symbol:RETREG1
Accession:XM_011514055
Location:INTRON

Gene Symbol:RETREG1
Accession:NM_019000
Location:INTRON

Gene Symbol:RETREG1
Accession:XM_011514053
Location:INTRON

Gene Symbol:RETREG1
Accession:NM_001034850
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001555346 CLINVAR
dbSNP (RS) rs75553033 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RETREG1 CLINVAR
OMIM 613114 CLINVAR