rs2551707 Rat Genome Database

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Variant: rs2551707 -  Homo sapiens

RGD ID: 150478896
RS ID: rs2551707
ClinVar ID: CV1218866
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GSR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 30,565,884
GRCh38 8 30,708,367
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1167t1:c.423-226T>C
NM_000637.5:c.423-226T>C
NM_001195102.3:c.423-226T>C
NM_001195103.3:c.423-226T>C
More... 		06/19/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GSR
Accession:XM_047421728
Location:5UTRS;EXON

Gene Symbol:GSR
Accession:NM_000637
Location:INTRON

Gene Symbol:GSR
Accession:NM_001195104
Location:INTRON

Gene Symbol:GSR
Accession:NM_001195103
Location:INTRON

Gene Symbol:GSR
Accession:NM_001195102
Location:INTRON

Gene Symbol:GSR
Accession:XM_047421727
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001616494 CLINVAR
dbSNP (RS) rs2551707 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GSR CLINVAR
OMIM 138300 CLINVAR