RGD:14745713 Rat Genome Database

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Variant: RGD:14745713 -  Homo sapiens

RGD ID: 14745713
RS ID: rs113395896
ClinVar ID: CV669020
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124904633  MYO1F  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 8,604,985
GRCh38 19 8,540,101
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012335.3:c.1611-73C>T
NM_001348355.2:c.1599-73C>T
NM_012335.4:c.1611-73C>T
NG_052844.1:g.42347C>T
More... 		06/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MYO1F
Accession:XM_047438852
Location:INTRON

Gene Symbol:MYO1F
Accession:NM_012335
Location:INTRON

Gene Symbol:MYO1F
Accession:XM_011528024
Location:INTRON

Gene Symbol:MYO1F
Accession:NM_001348355
Location:INTRON

Gene Symbol:MYO1F
Accession:XM_011528028
Location:INTRON

Gene Symbol:MYO1F
Accession:XM_011528027
Location:INTRON

Gene Symbol:LOC124904633
Accession:XR_007067130
Location:INTRON;NON-CODING

Gene Symbol:MYO1F
Accession:XR_936182
Location:INTRON;NON-CODING

Gene Symbol:MYO1F
Accession:XR_936181
Location:INTRON;NON-CODING

Gene Symbol:LOC124904633
Accession:XR_007067131
Location:INTRON;NON-CODING

Gene Symbol:MYO1F
Accession:XR_001753692
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000843665 CLINVAR
dbSNP (RS) rs113395896 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYO1F CLINVAR
OMIM 601480 CLINVAR