RGD:408379222 Rat Genome Database

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Variant: RGD:408379222 -  Homo sapiens

RGD ID: 408379222
ClinVar ID: CV3517114
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIGN  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 18 59,806,235
GRCh38 18 62,139,002
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000018.10:g.62139002T>A
NC_000018.9:g.59806235T>A
NM_176787.4:c.1097A>T
NP_036459.1:p.Gln366Leu
More... 		07/28/2024 missense variant uncertain significance PIGN-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004752641 CLINVAR
NCBI Gene PIGN CLINVAR
OMIM 606097 CLINVAR