Product Details

SNP ID

rs35762677

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:129675326 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACCAGCCCAAGGCAGCCCAGGGGC[G/T]TGGAATGCAGGGGTGATGTGATAGG

Phenotype

MIM: 604675

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

PRRX2 PubMed Links

Gene Details

Gene

PRRX2

Gene Name

paired related homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016307.3		Intron			NP_057391.1
XM_017014803.1		Intron			XP_016870292.1

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