Product Details

SNP ID

rs148094437

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:2855780 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCAGGCAACACCCACCTTCTGG[C/G]ACCGAGAGCCAGGGTTCCCCAGCTG

Phenotype

MIM: 609343

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PRSS22 PubMed Links

Gene Details

Gene

PRSS22

Gene Name

protease, serine 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022119.3	419	Missense Mutation	TCC,TGC	S118C	NP_071402.1
XM_005255473.3	419	Missense Mutation	TCC,TGC	S118C	XP_005255530.1

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