RGD:150444475 Rat Genome Database

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Variant: RGD:150444475 -  Homo sapiens

RGD ID: 150444475
RS ID: rs2306490
ClinVar ID: CV1216634
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYO9A  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 72,227,837
GRCh38 15 71,935,496
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006901.4:c.2379-12T>C
NC_000015.10:g.71935496A>G
NC_000015.9:g.72227837A>G
 05/04/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MYO9A
Accession:NM_006901
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_006720539
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521621
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432566
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432548
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432561
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432572
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432558
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521622
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521614
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432578
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432554
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_017022229
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432584
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521619
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521618
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432580
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432555
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521615
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432576
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432553
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432569
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432550
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521613
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432581
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432557
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432567
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432562
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521620
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432559
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432551
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432565
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432579
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521616
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_011521617
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432570
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432585
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432549
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432568
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432560
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432573
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432547
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432556
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432564
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432552
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_017022230
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432575
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432577
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432571
Location:INTRON

Gene Symbol:MYO9A
Accession:XM_047432583
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001610934 CLINVAR
dbSNP (RS) rs2306490 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYO9A CLINVAR
OMIM 604875 CLINVAR