RGD:405144211 Rat Genome Database

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Variant: RGD:405144211 -  Homo sapiens

RGD ID: 405144211
ClinVar ID: CV3027276
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126806490  UNC80  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 210,783,333
GRCh38 2 209,918,609
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_182587.4:c.5076G>T
NM_032504.2:c.5091G>T
NM_001371986.1:c.5289G>T
NG_082810.1:g.1023G>T
More... 		05/22/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003702778 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126806490 CLINVAR
  UNC80 CLINVAR
OMIM 612636 CLINVAR