Product Details

SNP ID

rs6104066

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:45221465 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAAGCAGCTGTGATGGGACAAAAA[A/G]GTGAGTGGAGAGGGTAAGCCTTGGG

Phenotype

MIM: 182141

Polymorphism

A/G, 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	97	Missense Mutation	AGT,GGT	S26G	NP_002999.1

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