Product Details

SNP ID

rs4900321

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:96283044 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAACACTGAGTTATCTAAAAGGCA[A/T]TGTTCAGTGGTGGGCAGAAAGGAAG

Phenotype

MIM: 616226

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

ATG2B PubMed Links

Additional Information

For this assay, SNP(s) [rs117614273] 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

ATG2B

Gene Name

autophagy related 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_006720187.2		Intron			XP_006720250.1
XM_017021397.1		Intron			XP_016876886.1

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