Product Details

SNP ID
rs201569191
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:57204691 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTTGGTTGGGCCGTGTTCTTAGC[A/G]AGCAGAAGCCTTGGCCAGGGTCTGT
Phenotype
MIM: 616585
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RSPRY1 PubMed Links

Gene Details

Gene
RSPRY1
Gene Name
ring finger and SPRY domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305163.1 356 Silent Mutation GCA,GCG A11A NP_001292092.1
NM_001305164.1 356 Silent Mutation GCA,GCG A11A NP_001292093.1
NM_001305182.1 356 Silent Mutation GCA,GCG A11A NP_001292111.1
NM_133368.2 356 Silent Mutation GCA,GCG A11A NP_588609.1
XM_005256220.1 356 Silent Mutation GCA,GCG A11A XP_005256277.1
XM_011523427.1 356 Silent Mutation GCA,GCG A11A XP_011521729.1
XM_011523428.1 356 Silent Mutation GCA,GCG A11A XP_011521730.1
XM_011523430.1 356 Silent Mutation GCA,GCG A11A XP_011521732.1
XM_017023844.1 356 UTR 5 XP_016879333.1

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