Product Details

SNP ID

rs138795111

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:18093889 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCAGCTCCTGGAACCGTCCAAATC[A/G]GCCTCGTCCAAAGGAGAGGGCTTTG

Phenotype

MIM: 602986

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DRG2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2230316] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

DRG2

Gene Name

developmentally regulated GTP binding protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001388.4	280	Silent Mutation	TCA,TCG	S47S	NP_001379.1
XM_005256499.2	280	Silent Mutation	TCA,TCG	S47S	XP_005256556.1
XM_005256500.2	280	UTR 5			XP_005256557.1
XM_011523704.1	280	Silent Mutation	TCA,TCG	S47S	XP_011522006.1
XM_011523705.1	280	Silent Mutation	TCA,TCG	S47S	XP_011522007.1
XM_011523706.1	280	UTR 5			XP_011522008.1
XM_011523707.1	280	UTR 5			XP_011522009.1
XM_017024296.1	280	UTR 5			XP_016879785.1
XM_017024297.1	280	UTR 5			XP_016879786.1

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