Product Details

SNP ID

rs2657880

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.12:56469986 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACTTGTTCTTGGGGCTCTACCAGAT[C/G]GCTGAAGAGTAAATCCTTTCTACCT

Phenotype

MIM: 606365

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

GLS2 PubMed Links

Additional Information

For this assay, SNP(s) [rs74811816] 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

GLS2

Gene Name

glutaminase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001280796.1	1108	Intron			NP_001267725.1
NM_001280797.1	1108	Intron			NP_001267726.1
NM_001280798.1	1108	Intron			NP_001267727.1
NM_013267.3	1108	Intron			NP_037399.2
XM_005268797.1	1108	Intron			XP_005268854.1
XM_017019180.1	1108	Intron			XP_016874669.1

Gene

SPRYD4

Gene Name

SPRY domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207344.3	1108	UTR 3			NP_997227.1

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