Product Details

SNP ID

rs199977814

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:30445402 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGCCCAGGGCTGGAAAGGTGGGG[C/T]TGGGGCCCGCTCCTGCCGGCAGGCC

Phenotype

MIM: 606218

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SEPHS2 PubMed Links

Gene Details

Gene

SEPHS2

Gene Name

selenophosphate synthetase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012248.3	574	Missense Mutation	AAC,AGC	N109S	NP_036380.2

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