RGD:407472118 Rat Genome Database

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Variant: RGD:407472118 -  Homo sapiens

RGD ID: 407472118
ClinVar ID: CV3446117
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRIG3  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 59,313,793
GRCh38 12 58,920,012
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_153377.5:c.224G>C
NG_186739.1:g.62C>G
NC_000012.12:g.58920012C>G
NC_000012.11:g.59313793C>G
More... 		03/25/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004637545 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LRIG3 CLINVAR
OMIM 608870 CLINVAR