RGD:150418011 Rat Genome Database

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Variant: RGD:150418011 -  Homo sapiens

RGD ID: 150418011
RS ID: rs185807432
ClinVar ID: CV1179292
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PGM1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 64,059,717
GRCh38 1 63,594,046
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016966.1:g.5771C>T
NC_000001.11:g.63594046C>T
NC_000001.10:g.64059717C>T
NM_001172819.2:c.-444C>T
More... 		10/02/2018 5 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PGM1
Accession:NM_001172819
Location:5UTRS;EXON

Gene Symbol:PGM1
Accession:NM_002633
Location:INTRON

Gene Symbol:PGM1
Accession:NM_001172818
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001550407 CLINVAR
dbSNP (RS) rs185807432 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PGM1 CLINVAR
OMIM 171900 CLINVAR