Product Details

SNP ID

rs147500806

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:8696471 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGCTCCCTGTCTTGGATGAAGCCA[A/G]CAAACATCTGAGACTCCATAAAAAC

Phenotype

MIM: 603637 MIM: 140750

Polymorphism

A/G, 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	3642	Missense Mutation	GCT,GTT	A1083V	NP_005409.3
NM_139157.2	3642	Missense Mutation	GCT,GTT	A663V	NP_631896.1
NM_213618.1	3642	Missense Mutation	GCT,GTT	A1083V	NP_998783.1
XM_005253077.1	3642	Missense Mutation	GCT,GTT	A1113V	XP_005253134.1
XM_005253083.2	3642	Missense Mutation	GCT,GTT	A663V	XP_005253140.1
XM_011520309.1	3642	Missense Mutation	GCT,GTT	A1133V	XP_011518611.1
XM_011520310.1	3642	Missense Mutation	GCT,GTT	A1123V	XP_011518612.1
XM_011520311.2	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518613.1
XM_011520312.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518614.1
XM_011520313.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518615.1
XM_011520314.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518616.1
XM_011520315.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518617.1
XM_011520316.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518618.1
XM_011520317.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_011518619.1
XM_011520318.1	3642	Missense Mutation	GCT,GTT	A1083V	XP_011518620.1
XM_011520319.2	3642	Missense Mutation	GCT,GTT	A923V	XP_011518621.1
XM_011520320.1	3642	Intron			XP_011518622.1
XM_011520321.2	3642	Intron			XP_011518623.1
XM_011520322.1	3642	Intron			XP_011518624.1
XM_011520323.2	3642	Missense Mutation	GCT,GTT	A713V	XP_011518625.2
XM_011520324.2	3642	Missense Mutation	GCT,GTT	A693V	XP_011518626.2
XM_011520325.1	3642	Missense Mutation	GCT,GTT	A683V	XP_011518627.1
XM_011520326.1	3642	Missense Mutation	GCT,GTT	A683V	XP_011518628.1
XM_011520327.1	3642	Missense Mutation	GCT,GTT	A683V	XP_011518629.1
XM_011520328.1	3642	Missense Mutation	GCT,GTT	A683V	XP_011518630.1
XM_011520329.1	3642	Missense Mutation	GCT,GTT	A663V	XP_011518631.1
XM_017018182.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_016873671.1
XM_017018183.1	3642	Missense Mutation	GCT,GTT	A1103V	XP_016873672.1
XM_017018184.1	3642	Missense Mutation	GCT,GTT	A923V	XP_016873673.1
XM_017018185.1	3642	Missense Mutation	GCT,GTT	A923V	XP_016873674.1
XM_017018186.1	3642	Missense Mutation	GCT,GTT	A903V	XP_016873675.1
XM_017018187.1	3642	Missense Mutation	GCT,GTT	A683V	XP_016873676.1

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