Product Details

SNP ID

rs190800927

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:71826742 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTTAATTTTTGTTTGCCCTTTTC[C/T]GGGTTGAAGGTTCCTCTGCTGATGA

Phenotype

MIM: 604875 MIM: 604485

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO9A PubMed Links

Gene Details

Gene

MYO9A

Gene Name

myosin IXA

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006901.3	7932	Silent Mutation	CCA,CCG	P2495P	NP_008832.2
XM_006720539.2	7932	Silent Mutation	CCA,CCG	P2566P	XP_006720602.1
XM_011521613.2	7932	Silent Mutation	CCA,CCG	P2585P	XP_011519915.1
XM_011521614.2	7932	Silent Mutation	CCA,CCG	P2585P	XP_011519916.1
XM_011521615.2	7932	Silent Mutation	CCA,CCG	P2585P	XP_011519917.1
XM_011521616.2	7932	Silent Mutation	CCA,CCG	P2585P	XP_011519918.1
XM_011521617.2	7932	Silent Mutation	CCA,CCG	P2584P	XP_011519919.1
XM_011521618.2	7932	Silent Mutation	CCA,CCG	P2567P	XP_011519920.1
XM_011521619.2	7932	Silent Mutation	CCA,CCG	P2566P	XP_011519921.1
XM_011521620.2	7932	Silent Mutation	CCA,CCG	P2565P	XP_011519922.1
XM_011521621.2	7932	Silent Mutation	CCA,CCG	P2545P	XP_011519923.1
XM_011521622.2	7932	Silent Mutation	CCA,CCG	P2513P	XP_011519924.1
XM_011521623.2	7932	Silent Mutation	CCA,CCG	P1684P	XP_011519925.1
XM_017022228.1	7932	Silent Mutation	CCA,CCG	P2566P	XP_016877717.1
XM_017022229.1	7932	Silent Mutation	CCA,CCG	P2513P	XP_016877718.1
XM_017022230.1	7932	Silent Mutation	CCA,CCG	P2494P	XP_016877719.1

Gene

NR2E3

Gene Name

nuclear receptor subfamily 2 group E member 3

There are no transcripts associated with this gene.

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