RGD:405083784 Rat Genome Database

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Variant: RGD:405083784 -  Homo sapiens

RGD ID: 405083784
ClinVar ID: CV3167164
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MID1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 10,534,915
GRCh38 X 10,566,875
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001193280.1:c.546+127C>T
NM_033289.2:c.546+127C>T
NM_000381.4:c.660+13C>T
NM_001098624.2:c.660+13C>T
More... 		01/05/2024 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MID1
Accession:NM_001193280
Location:INTRON

Gene Symbol:MID1
Accession:NM_001347733
Location:INTRON

Gene Symbol:MID1
Accession:NM_000381
Location:INTRON

Gene Symbol:MID1
Accession:NM_001193277
Location:INTRON

Gene Symbol:MID1
Accession:NM_001193279
Location:INTRON

Gene Symbol:MID1
Accession:NM_001193278
Location:INTRON

Gene Symbol:MID1
Accession:NM_033290
Location:INTRON

Gene Symbol:MID1
Accession:NM_001098624
Location:INTRON

Gene Symbol:MID1
Accession:NM_033289
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003851743 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MID1 CLINVAR
OMIM 300552 CLINVAR