Product Details

SNP ID
rs141330508
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:132208062 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGCCGCACATGGGCAGGGCGGAG[C/T]GTTCCGCCTCGTCCTCCACAGGCTC
Phenotype
MIM: 608407
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
DPYSL4 PubMed Links
Additional Information
For this assay, SNP(s) [rs79220014] 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
DPYSL4
Gene Name
dihydropyrimidinase like 4
There are no transcripts associated with this gene.

Gene
STK32C
Gene Name
serine/threonine kinase 32C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318878.1 1620 Missense Mutation CAC,CGC H483R NP_001305807.1
NM_001318879.1 1620 Missense Mutation CAC,CGC H353R NP_001305808.1
NM_001318880.1 1620 Intron NP_001305809.1
NM_001318881.1 1620 Intron NP_001305810.1
NM_001318882.1 1620 Intron NP_001305811.1
NM_001318883.1 1620 Intron NP_001305812.1
NM_173575.3 1620 Missense Mutation CAC,CGC H470R NP_775846.2
XM_011539688.1 1620 Missense Mutation CAC,CGC H488R XP_011537990.1
XM_011539690.2 1620 Missense Mutation CAC,CGC H475R XP_011537992.1
XM_011539693.2 1620 Missense Mutation CAC,CGC H353R XP_011537995.1
XM_011539694.1 1620 Missense Mutation CAC,CGC H353R XP_011537996.1
XM_011539695.1 1620 Missense Mutation CAC,CGC H353R XP_011537997.1
XM_011539696.1 1620 Missense Mutation CAC,CGC H353R XP_011537998.1
XM_017016100.1 1620 Intron XP_016871589.1
XM_017016101.1 1620 Intron XP_016871590.1

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