Product Details

SNP ID
rs149922066
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:166929662 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGACTCTCAGACCCCGGCTCTCGG[C/T]GGCCCCATTTGCCAGCCAGACTTCC
Phenotype
MIM: 612944
Polymorphism
C/T, 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 1104 Missense Mutation NP_003721.2
XM_017011397.1 1104 Intron XP_016866886.1
XM_017011398.1 1104 Intron XP_016866887.1
XM_017011399.1 1104 UTR 3 XP_016866888.1

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