Product Details

SNP ID

rs2925651

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:72125641 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAATAAAGTACTGATAGATATTCCT[C/T]CAAAAAAAAGAAAGACTATTTCGTG

Phenotype

MIM: 604875 MIM: 608659

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYO9A PubMed Links

Additional Information

For this assay, SNP(s) [rs149649570] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

MYO9A

Gene Name

myosin IXA

There are no transcripts associated with this gene.

Gene

SENP8

Gene Name

SUMO/sentrin peptidase family member, NEDD8 specific

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166340.1		Intron			NP_001159812.1
NM_001172109.1		Intron			NP_001165580.1
NM_001172110.1		Intron			NP_001165581.1
NM_001172111.1		Intron			NP_001165582.1
NM_145204.3		Intron			NP_660205.3
XM_005254157.3		Intron			XP_005254214.1
XM_011521215.2		Intron			XP_011519517.1
XM_011521217.2		Intron			XP_011519519.1

View Full Product Details