Product Details

SNP ID

rs2233899

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:45222159 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTCATGGACTAAGTAAAGAACAAG[C/T]TTCAGCCTCTGGTGCACAAAAAGGT

Phenotype

MIM: 182141

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SEMG2 PubMed Links

Gene Details

Gene

SEMG2

Gene Name

semenogelin II

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003008.2	548	Missense Mutation	GCT,GTT	A176V	NP_002999.1

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