Product Details

SNP ID

rs150076785

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:2818817 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATCTGAGCCCTCGCTACCTGGGGA[A/G]TTCACCCTATGACATTGCCTTGGTG

Phenotype

MIM: 608159

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PRSS21 PubMed Links

Additional Information

For this assay, SNP(s) [rs2074906] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

PRSS21

Gene Name

protease, serine 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270452.1	424	Missense Mutation	AAT,AGT	N131S	NP_001257381.1
NM_006799.3	424	Missense Mutation	AAT,AGT	N133S	NP_006790.1
NM_144956.2	424	Missense Mutation	AAT,AGT	N131S	NP_659205.1
NM_144957.2	424	Missense Mutation	AAT,AGT	N133S	NP_659206.1
XM_017022875.1	424	Missense Mutation	AAT,AGT	N131S	XP_016878364.1
XM_017022876.1	424	Missense Mutation	AAT,AGT	N133S	XP_016878365.1
XM_017022877.1	424	Missense Mutation	AAT,AGT	N131S	XP_016878366.1
XM_017022878.1	424	Missense Mutation	AAT,AGT	N133S	XP_016878367.1

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