RGD:405290026 Rat Genome Database

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Variant: RGD:405290026 -  Homo sapiens

RGD ID: 405290026
ClinVar ID: CV3214030
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127458247  MNX1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 156,798,207
GRCh38 7 157,005,513
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001165255.2:c.*7C>G
NM_005515.4:c.*7C>G
NG_013212.1:g.10141C>G
NG_113020.1:g.333G>C
More... 		09/11/2019 3 prime utr variant likely benign MNX1-related condition

Variant Details
Variant Transcripts
Gene Symbol:MNX1
Accession:NM_005515
Location:3UTRS;EXON

Gene Symbol:MNX1
Accession:NM_001165255
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003926875 CLINVAR
NCBI Gene MNX1 CLINVAR
OMIM 142994 CLINVAR