RGD:11606282 Rat Genome Database

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Variant: RGD:11606282 -  Homo sapiens

RGD ID: 11606282
ClinVar ID: CV318086
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127824361  MYO1A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 57,423,379
GRCh38 12 57,029,595
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012104.1:g.25515G>A
NC_000012.12:g.57029595C>T
NC_000012.11:g.57423379C>T
NM_005379.3:c.2725-8G>A
More... 		06/14/2016 intron variant uncertain significance

Variant Details
Variant Transcripts
Gene Symbol:MYO1A
Accession:XM_047428876
Location:INTRON

Gene Symbol:MYO1A
Accession:NM_005379
Location:INTRON

Gene Symbol:MYO1A
Accession:NM_001256041
Location:INTRON

Gene Symbol:MYO1A
Accession:XM_011538373
Location:INTRON

Variant Samples