Product Details

SNP ID

rs13213697

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:166931095 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGGGTATCACTCCATATACTCTGGC[A/G]AGGGCATCTTTAAAATCTGCAACCT

Phenotype

MIM: 612944

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNASET2 PubMed Links

Gene Details

Gene

RNASET2

Gene Name

ribonuclease T2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003730.4	923	Silent Mutation	CTC,CTT	L172L	NP_003721.2
XM_017011397.1	923	Intron			XP_016866886.1
XM_017011398.1	923	Intron			XP_016866887.1
XM_017011399.1	923	Missense Mutation	TCG,TTG	S157L	XP_016866888.1

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