RGD:407487202 Rat Genome Database

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Variant: RGD:407487202 -  Homo sapiens

RGD ID: 407487202
ClinVar ID: CV3479897
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ROR2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 94,495,502
GRCh38 9 91,733,220
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001318204.2:c.839G>A
NM_004560.4:c.839G>A
NG_008089.1:g.221943G>A
NC_000009.12:g.91733220C>T
More... 		03/30/2024 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004665620 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene ROR2 CLINVAR
OMIM 602337 CLINVAR