RGD:405162018 Rat Genome Database

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Variant: RGD:405162018 -  Homo sapiens

RGD ID: 405162018
ClinVar ID: CV3153027
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MID1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 10,423,113
GRCh38 X 10,455,073
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_033289.2:c.1338A>G
NM_000381.4:c.1452A>G
NM_001098624.2:c.1452A>G
NM_001193277.1:c.1452A>G
More... 		12/09/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003840762 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MID1 CLINVAR
OMIM 300552 CLINVAR