Product Details

SNP ID

rs137996775

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:8696435 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGATAACCAAGACTTACCCTTTGCC[C/T]GACACTTTCTTAGCTCCCTGTCTTG

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	3678	Missense Mutation			NP_005409.3
NM_139157.2	3678	Missense Mutation			NP_631896.1
NM_213618.1	3678	Missense Mutation			NP_998783.1
XM_005253077.1	3678	Missense Mutation			XP_005253134.1
XM_005253083.2	3678	Missense Mutation			XP_005253140.1
XM_011520309.1	3678	Missense Mutation			XP_011518611.1
XM_011520310.1	3678	Missense Mutation			XP_011518612.1
XM_011520311.2	3678	Missense Mutation			XP_011518613.1
XM_011520312.1	3678	Missense Mutation			XP_011518614.1
XM_011520313.1	3678	Missense Mutation			XP_011518615.1
XM_011520314.1	3678	Missense Mutation			XP_011518616.1
XM_011520315.1	3678	Missense Mutation			XP_011518617.1
XM_011520316.1	3678	Missense Mutation			XP_011518618.1
XM_011520317.1	3678	Missense Mutation			XP_011518619.1
XM_011520318.1	3678	Missense Mutation			XP_011518620.1
XM_011520319.2	3678	Missense Mutation			XP_011518621.1
XM_011520320.1	3678	Intron			XP_011518622.1
XM_011520321.2	3678	Intron			XP_011518623.1
XM_011520322.1	3678	Intron			XP_011518624.1
XM_011520323.2	3678	Missense Mutation			XP_011518625.2
XM_011520324.2	3678	Missense Mutation			XP_011518626.2
XM_011520325.1	3678	Missense Mutation			XP_011518627.1
XM_011520326.1	3678	Missense Mutation			XP_011518628.1
XM_011520327.1	3678	Missense Mutation			XP_011518629.1
XM_011520328.1	3678	Missense Mutation			XP_011518630.1
XM_011520329.1	3678	Missense Mutation			XP_011518631.1
XM_017018182.1	3678	Missense Mutation			XP_016873671.1
XM_017018183.1	3678	Missense Mutation			XP_016873672.1
XM_017018184.1	3678	Missense Mutation			XP_016873673.1
XM_017018185.1	3678	Missense Mutation			XP_016873674.1
XM_017018186.1	3678	Missense Mutation			XP_016873675.1
XM_017018187.1	3678	Missense Mutation			XP_016873676.1

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