Product Details

SNP ID
rs9581165
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:24751584 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAAGGTTCAAGTAAAGACTCTGAAG[C/T]AGTCTCAGGGATATACTGCTTGGTA
Phenotype
MIM: 605793
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF17 PubMed Links

Gene Details

Gene
RNF17
Gene Name
ring finger protein 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184993.1 359 Intron NP_001171922.1
NM_031277.2 359 Intron NP_112567.2
XM_006719846.3 359 Intron XP_006719909.1
XM_006719849.2 359 Intron XP_006719912.1
XM_006719852.2 359 Intron XP_006719915.1
XM_011535152.2 359 UTR 5 XP_011533454.1
XM_011535155.2 359 Intron XP_011533457.1
XM_011535156.2 359 UTR 5 XP_011533458.1
XM_011535157.2 359 UTR 5 XP_011533459.1
XM_011535158.2 359 UTR 5 XP_011533460.1
XM_011535159.2 359 UTR 5 XP_011533461.1
XM_011535160.2 359 UTR 5 XP_011533462.1
XM_011535162.1 359 Intron XP_011533464.1
XM_011535163.1 359 Intron XP_011533465.1
XM_011535164.2 359 Intron XP_011533466.1
XM_017020676.1 359 Intron XP_016876165.1

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