Product Details

SNP ID
rs139749033
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:17044639 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGTTTCCTGGTTATTCTAAGCAA[C/T]TGTCAAAATTGGTAAATTTACACCT
Phenotype
MIM: 612935
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
MPRIP PubMed Links
Additional Information
For this assay, SNP(s) [rs141125761] are located under a primer 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
MPRIP
Gene Name
myosin phosphatase Rho interacting protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015134.3 Intron NP_055949.2
NM_201274.3 Intron NP_958431.2
XM_005256563.4 Intron XP_005256620.1
XM_005256564.4 Intron XP_005256621.3
XM_011523761.2 Intron XP_011522063.1
XM_011523762.2 Intron XP_011522064.1
XM_011523763.2 Intron XP_011522065.1
XM_011523764.2 Intron XP_011522066.1
XM_011523765.2 Intron XP_011522067.1
XM_011523766.2 Intron XP_011522068.2
XM_011523767.2 Intron XP_011522069.2
XM_017024393.1 Intron XP_016879882.1

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