RGD:407532361 Rat Genome Database

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Variant: RGD:407532361 -  Homo sapiens

RGD ID: 407532361
ClinVar ID: CV3493026
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TUBGCP5  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 22,850,952
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354374.2:c.1172G>A
NM_001102610.2:c.1214G>A
NM_001354373.2:c.1214G>A
NM_001354375.2:c.1214G>A
More... 		04/15/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004683005 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TUBGCP5 CLINVAR
OMIM 608147 CLINVAR