Product Details

SNP ID

rs146602887

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:57471504 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCTGTCCCTGGGCCTCTTGTTCAT[A/G]AAGCCATGTTTCCATTTTGCCAATT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C14orf105 PubMed Links

Additional Information

For this assay, SNP(s) [rs1152530] 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

C14orf105

Gene Name

chromosome 14 open reading frame 105

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001283056.1	1010	Missense Mutation	CAT,TAT	H288Y	NP_001269985.1
NM_001283057.1	1010	Missense Mutation	CAT,TAT	H247Y	NP_001269986.1
NM_001283058.1	1010	Missense Mutation	CAT,TAT	H159Y	NP_001269987.1
NM_001283059.1	1010	Missense Mutation	CAT,TAT	H159Y	NP_001269988.1
NM_001283060.1	1010	Intron			NP_001269989.1
NM_018168.3	1010	Missense Mutation	CAT,TAT	H248Y	NP_060638.2
XM_005267806.1	1010	Intron			XP_005267863.1
XM_005267810.3	1010	Missense Mutation	CAT,TAT	H169Y	XP_005267867.1
XM_005267811.3	1010	Missense Mutation	CAT,TAT	H160Y	XP_005267868.1
XM_005267813.1	1010	Missense Mutation	CAT,TAT	H122Y	XP_005267870.1
XM_005267814.1	1010	Missense Mutation	CAT,TAT	H121Y	XP_005267871.1
XM_006720188.2	1010	Intron			XP_006720251.1
XM_006720189.2	1010	Missense Mutation	CAT,TAT	H170Y	XP_006720252.1

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