RGD:597761818 Rat Genome Database

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Variant: RGD:597761818 -  Homo sapiens

RGD ID: 597761818
ClinVar ID: CV3685812
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HHLA1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 133,107,811
GRCh38 8 132,095,564
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001145095.3:c.403A>C
NC_000008.11:g.132095564T>G
NC_000008.10:g.133107811T>G
NM_001145095.1:c.403A>C
More... 		07/01/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004925993 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene HHLA1 CLINVAR
OMIM 604109 CLINVAR