Product Details

SNP ID

rs148905318

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:45222100 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAGCCCATCTGGAAAGGGATTATC[C/T]AGTCAATGTTCAAACACAGAAAAAA

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	489	Silent Mutation	TCC,TCT	S156S	NP_002999.1

View Full Product Details