Product Details

SNP ID

rs116634328

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:78170963 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGGGGTGCTGGCCTTCCTGGCCTC[A/G]GCCTTCTTCTTGGTGGTCGACGCGT

Phenotype

MIM: 603926 MIM: 188300

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C17orf99 PubMed Links

Additional Information

For this assay, SNP(s) [rs1062668] are located under a probe 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

C17orf99

Gene Name

chromosome 17 open reading frame 99

There are no transcripts associated with this gene.

Gene

SYNGR2

Gene Name

synaptogyrin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320523.1	318	Silent Mutation	TCA,TCG	S82S	NP_001307452.1
NM_004710.4	318	Silent Mutation	TCA,TCG	S82S	NP_004701.1
XM_005257792.3	318	Intron			XP_005257849.1

Gene

TK1

Gene Name

thymidine kinase 1

There are no transcripts associated with this gene.

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