Product Details

SNP ID

rs143908336

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:187670213 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAACTGACGGAGTCTGGGGTCCG[A/G]GGGAGCGCCGGTGACACAGCCCAGG

Phenotype

MIM: 182450

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SST PubMed Links

Gene Details

Gene

SST

Gene Name

somatostatin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001048.3	201	Missense Mutation	CCG,TCG	P27S	NP_001039.1

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