Product Details

SNP ID

rs139080890

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:11982418 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTAAGTTCCTGGATGCTCCTTTC[C/T]ATCAGTTTTTTTTTTTTTTTTTTTG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SNX29 PubMed Links

Additional Information

For this assay, SNP(s) [rs60761477] 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

SNX29

Gene Name

sorting nexin 29

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032167.4		Intron			NP_115543.3
XM_005255682.3		Intron			XP_005255739.1
XM_005255683.3		Intron			XP_005255740.1
XM_011522738.2		Intron			XP_011521040.1
XM_011522741.2		Intron			XP_011521043.1
XM_011522743.2		Intron			XP_011521045.1
XM_011522744.2		Intron			XP_011521046.1
XM_017023871.1		Intron			XP_016879360.1
XM_017023872.1		Intron			XP_016879361.1
XM_017023873.1		Intron			XP_016879362.1
XM_017023874.1		Intron			XP_016879363.1
XM_017023875.1		Intron			XP_016879364.1
XM_017023876.1		Intron			XP_016879365.1
XM_017023877.1		Intron			XP_016879366.1
XM_017023878.1		Intron			XP_016879367.1

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