RGD:405165365 Rat Genome Database

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Variant: RGD:405165365 -  Homo sapiens

RGD ID: 405165365
ClinVar ID: CV3059528
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MID1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 10,450,611
GRCh38 X 10,482,571
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001193278.1:c.1075C>T
NM_001193280.1:c.808C>T
NM_033289.2:c.808C>T
NM_000381.4:c.922C>T
More... 		01/16/2024 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003727399 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MID1 CLINVAR
OMIM 300552 CLINVAR