Product Details

SNP ID

rs645196

Assay Type

Functionally tested

NCBI dbSNP Submissions

39

Location

Chr.1:170663925 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGACTTTTTAATATTGTATTTTA[C/G]TGTGGATTATCTCTTTGGACCGCGC

Phenotype

MIM: 167420

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PRRX1 PubMed Links

Gene Details

Gene

PRRX1

Gene Name

paired related homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006902.4		Intron			NP_008833.1
NM_022716.3		Intron			NP_073207.1
XM_006711388.3		Intron			XP_006711451.1

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