Product Details

SNP ID

rs199823417

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:166929654 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCTTCACAGACTCTCAGACCCCG[G/T]CTCTCGGCGGCCCCATTTGCCAGCC

Phenotype

MIM: 612944

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

RNASET2 PubMed Links

Additional Information

For this assay, SNP(s) [rs11159] are located under a probe 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

RNASET2

Gene Name

ribonuclease T2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003730.4	1112	Missense Mutation	AGA,AGC	R235S	NP_003721.2
XM_017011397.1	1112	Intron			XP_016866886.1
XM_017011398.1	1112	Intron			XP_016866887.1
XM_017011399.1	1112	UTR 3			XP_016866888.1

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