Product Details

SNP ID

rs74613026

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:114281835 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAACCTCGCGAGGAGAAGAGGACG[G/T]CCCTGAGCAAGGTGGGGACGGGGGC

Phenotype

MIM: 603461 MIM: 605530

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CDC16 PubMed Links

Additional Information

For this assay, SNP(s) [rs556799572] 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

CDC16

Gene Name

cell division cycle 16

There are no transcripts associated with this gene.

Gene

MIR4502

Gene Name

microRNA 4502

There are no transcripts associated with this gene.

Gene

UPF3A

Gene Name

UPF3 regulator of nonsense transcripts homolog A (yeast)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023011.3	252	Missense Mutation	GCC,TCC	A66S	NP_075387.1
NM_080687.2	252	Missense Mutation	GCC,TCC	A66S	NP_542418.1
XM_005266202.4	252	Intron			XP_005266259.1
XM_006719991.3	252	Intron			XP_006720054.1
XM_011534844.1	252	Intron			XP_011533146.1
XM_011534845.2	252	Intron			XP_011533147.1
XM_011534846.1	252	Missense Mutation	GCC,TCC	A66S	XP_011533148.1
XM_011534847.2	252	Intron			XP_011533149.1
XM_011534848.2	252	Intron			XP_011533150.1
XM_017020709.1	252	Intron			XP_016876198.1
XM_017020710.1	252	Intron			XP_016876199.1
XM_017020711.1	252	Intron			XP_016876200.1
XM_017020712.1	252	Missense Mutation	GCC,TCC	A66S	XP_016876201.1

View Full Product Details