Product Details

SNP ID
rs79908606
Assay Type
Functionally tested
NCBI dbSNP Submissions
14
Location
Chr.1:170666075 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTAGTTCTAACAAAATGCACTGA[G/T]AAATACTATGATTGTTTTTAAACGT
Phenotype
MIM: 167420
Polymorphism
G/T, 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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