RGD:8637635 Rat Genome Database

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Variant: RGD:8637635 -  Homo sapiens

RGD ID: 8637635
ClinVar ID: CV92861
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MPST  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 37,421,009
GRCh38 22 37,024,968
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000022.9:g.35750955C>A
NC_000022.11:g.37024968C>A
NC_000022.10:g.37421009C>A
NM_021126.4:c.595+158C>A
More... 		intron|intron variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:MPST
Accession:NM_001369905
Location:INTRON

Gene Symbol:MPST
Accession:XM_047441377
Location:INTRON

Gene Symbol:MPST
Accession:NM_001130517
Location:INTRON

Gene Symbol:MPST
Accession:NM_001013436
Location:INTRON

Gene Symbol:MPST
Accession:NM_001369904
Location:INTRON

Gene Symbol:MPST
Accession:NM_021126
Location:INTRON

Gene Symbol:MPST
Accession:XM_047441376
Location:INTRON

Variant Samples