RGD:8645116 Rat Genome Database

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Variant: RGD:8645116 -  Homo sapiens

RGD ID: 8645116
RS ID: rs281865179
ClinVar ID: CV104520
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GPR143  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 9,728,752
GRCh38 X 9,760,712
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009074.1:g.10166G>C
NC_000023.11:g.9760712C>G
NC_000023.10:g.9728752C>G
NM_000273.3:c.360+5G>C
More... 		04/01/2022 intron|intron variant likely pathogenic|not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:GPR143
Accession:NM_000273
Location:INTRON

Gene Symbol:GPR143
Accession:XM_024452388
Location:INTRON

Gene Symbol:GPR143
Accession:XM_005274541
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000084927 CLINVAR
dbSNP (RS) rs281865179 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GPR143 CLINVAR
OMIM 300808 CLINVAR