RGD:407521539 Rat Genome Database

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Variant: RGD:407521539 -  Homo sapiens

RGD ID: 407521539
ClinVar ID: CV3437071
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HEPHL1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 93,837,734
GRCh38 11 94,104,568
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001098672.2:c.2723G>T
NC_000011.10:g.94104568G>T
NC_000011.9:g.93837734G>T
NM_001098672.1:c.2723G>T
More... 		03/15/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004630396 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene HEPHL1 CLINVAR
OMIM 618455 CLINVAR