rs1187889736 Rat Genome Database

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Variant: rs1187889736 -  Homo sapiens

RGD ID: 152978746
RS ID: rs1187889736
ClinVar ID: CV1673803
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADSS1  LOC124903396  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 105,201,341
GRCh38 14 104,735,004
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_199165.2:c.322-16C>T
NG_051175.1:g.15808C>T
NC_000014.9:g.104735004C>T
NC_000014.8:g.105201341C>T
More... 		11/15/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:ADSS1
Accession:NM_001320424
Location:5UTRS;INTRON

Gene Symbol:LOC124903396
Accession:XR_007064365
Location:EXON;NON-CODING

Gene Symbol:ADSS1
Accession:NM_152328
Location:INTRON

Gene Symbol:ADSS1
Accession:NM_199165
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_006720026
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_011536412
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_047430917
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_047430916
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002236658 CLINVAR
dbSNP (RS) rs1187889736 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ADSS1 CLINVAR
OMIM 612498 CLINVAR