RGD:405169773 Rat Genome Database

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Variant: RGD:405169773 -  Homo sapiens

RGD ID: 405169773
ClinVar ID: CV2854223
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLA  TG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 134,107,311
GRCh38 8 133,095,067
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_003226.4:p.Ala2421=
NM_001282965.2:c.-264+7486G>A
NM_001045556.3:c.-319+7486G>A
NG_015832.1:g.233107C>T
More... 		01/24/2024 intron variant likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003542071 CLINVAR
  RCV003919252 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLA CLINVAR
  TG CLINVAR
OMIM 188450 CLINVAR
  601099 CLINVAR