RGD:401930737 Rat Genome Database

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Variant: RGD:401930737 -  Homo sapiens

RGD ID: 401930737
ClinVar ID: CV2828504
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYC  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 128,748,577
GRCh38 8 127,736,331
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1397t1:c.-263G>A
NM_001354870.1:c.-263G>A
NM_002467.6:c.-263G>A
LRG_1397:g.5898G>A
More... 		09/01/2023 5 prime utr variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Variant Details
Variant Transcripts
Gene Symbol:MYC
Accession:NM_002467
Location:5UTRS;EXON

Gene Symbol:MYC
Accession:NM_001354870
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003440637 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYC CLINVAR
OMIM 190080 CLINVAR