Product Details

SNP ID
rs149828734
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:8696649 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGATAAACACCTCCGACACCAGCC[C/T]ATTGAGGGTATTACATTCTGGAAGG
Phenotype
MIM: 603637 MIM: 140750
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RPL27A PubMed Links

Gene Details

Gene
RPL27A
Gene Name
ribosomal protein L27a
There are no transcripts associated with this gene.

Gene
ST5
Gene Name
suppression of tumorigenicity 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005418.3 3464 Missense Mutation AGG,GGG R1024G NP_005409.3
NM_139157.2 3464 Missense Mutation AGG,GGG R604G NP_631896.1
NM_213618.1 3464 Missense Mutation AGG,GGG R1024G NP_998783.1
XM_005253077.1 3464 Missense Mutation AGG,GGG R1054G XP_005253134.1
XM_005253083.2 3464 Missense Mutation AGG,GGG R604G XP_005253140.1
XM_011520309.1 3464 Missense Mutation AGG,GGG R1074G XP_011518611.1
XM_011520310.1 3464 Missense Mutation AGG,GGG R1064G XP_011518612.1
XM_011520311.2 3464 Missense Mutation AGG,GGG R1044G XP_011518613.1
XM_011520312.1 3464 Missense Mutation AGG,GGG R1044G XP_011518614.1
XM_011520313.1 3464 Missense Mutation AGG,GGG R1044G XP_011518615.1
XM_011520314.1 3464 Missense Mutation AGG,GGG R1044G XP_011518616.1
XM_011520315.1 3464 Missense Mutation AGG,GGG R1044G XP_011518617.1
XM_011520316.1 3464 Missense Mutation AGG,GGG R1044G XP_011518618.1
XM_011520317.1 3464 Missense Mutation AGG,GGG R1044G XP_011518619.1
XM_011520318.1 3464 Missense Mutation AGG,GGG R1024G XP_011518620.1
XM_011520319.2 3464 Missense Mutation AGG,GGG R864G XP_011518621.1
XM_011520320.1 3464 Intron XP_011518622.1
XM_011520321.2 3464 Intron XP_011518623.1
XM_011520322.1 3464 Intron XP_011518624.1
XM_011520323.2 3464 Missense Mutation AGG,GGG R654G XP_011518625.2
XM_011520324.2 3464 Missense Mutation AGG,GGG R634G XP_011518626.2
XM_011520325.1 3464 Missense Mutation AGG,GGG R624G XP_011518627.1
XM_011520326.1 3464 Missense Mutation AGG,GGG R624G XP_011518628.1
XM_011520327.1 3464 Missense Mutation AGG,GGG R624G XP_011518629.1
XM_011520328.1 3464 Missense Mutation AGG,GGG R624G XP_011518630.1
XM_011520329.1 3464 Missense Mutation AGG,GGG R604G XP_011518631.1
XM_017018182.1 3464 Missense Mutation AGG,GGG R1044G XP_016873671.1
XM_017018183.1 3464 Missense Mutation AGG,GGG R1044G XP_016873672.1
XM_017018184.1 3464 Missense Mutation AGG,GGG R864G XP_016873673.1
XM_017018185.1 3464 Missense Mutation AGG,GGG R864G XP_016873674.1
XM_017018186.1 3464 Missense Mutation AGG,GGG R844G XP_016873675.1
XM_017018187.1 3464 Missense Mutation AGG,GGG R624G XP_016873676.1

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