RGD:405225175 Rat Genome Database

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Variant: RGD:405225175 -  Homo sapiens

RGD ID: 405225175
ClinVar ID: CV3142313
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126863207  MID1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 10,417,510
GRCh38 X 10,449,470
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.1788G>A
NM_000381.4:c.1902G>A
NM_001098624.2:c.1902G>A
NM_001193277.1:c.1902G>A
More... 		09/20/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003847852 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126863207 CLINVAR
  MID1 CLINVAR
OMIM 300552 CLINVAR