RGD:13462832 Rat Genome Database

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Variant: RGD:13462832 -  Homo sapiens

RGD ID: 13462832
RS ID: rs141574483
ClinVar ID: CV439053
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MID2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 107,084,632
GRCh38 X 107,841,402
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000023.10:g.107084632G>A
NC_000023.11:g.107841402G>A
NM_012216.4:c.720+17G>A
NM_052817.3:c.720+17G>A
More... 		06/15/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MID2
Accession:NM_052817
Location:INTRON

Gene Symbol:MID2
Accession:NM_001382752
Location:INTRON

Gene Symbol:MID2
Accession:NM_001382751
Location:INTRON

Gene Symbol:MID2
Accession:NM_012216
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000514913 CLINVAR
dbSNP (RS) rs141574483 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MID2 CLINVAR
OMIM 300204 CLINVAR