RGD:597642774 Rat Genome Database

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Variant: RGD:597642774 -  Homo sapiens

RGD ID: 597642774
ClinVar ID: CV3692984
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LIMD1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 45,637,585
GRCh38 3 45,596,093
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014240.3:c.1214C>T
NC_000003.12:g.45596093C>T
NC_000003.11:g.45637585C>T
NM_014240.2:c.1214C>T
More... 		10/19/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004941949 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LIMD1 CLINVAR
OMIM 604543 CLINVAR