Product Details

SNP ID

rs116046664

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:2596719 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTAAGCCTCACCTTCCCTTTTAC[C/T]TATTTGTGCTGCTTCAGCCTCTTCG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM193A PubMed Links

Additional Information

For this assay, SNP(s) [rs113378414] 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

FAM193A

Gene Name

family with sequence similarity 193 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256666.1		Intron			NP_001243595.1
NM_001256667.1		Intron			NP_001243596.1
NM_001256668.1		Intron			NP_001243597.1
NM_003704.3		Intron			NP_003695.3
XM_006713930.2		Intron			XP_006713993.2
XM_006713932.2		Intron			XP_006713995.2
XM_011513590.1		Intron			XP_011511892.1
XM_011513593.2		Intron			XP_011511895.1
XM_017008788.1		Intron			XP_016864277.1

View Full Product Details