Product Details

SNP ID

rs191324911

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:38086320 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAAGGGTGGAGGTGCAGGGCTGGG[A/G]GCACGGCTTGGCACCCGGCTTGGGG

Phenotype

MIM: 610409

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

BAIAP2L2 PubMed Links

Additional Information

For this assay, SNP(s) [rs66500630] are located under a primer 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

BAIAP2L2

Gene Name

BAI1 associated protein 2 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025045.5	1815	Silent Mutation	GCC,GCT	A463A	NP_079321.3
XM_005261751.4	1815	Silent Mutation	GCC,GCT	A463A	XP_005261808.1
XM_011530379.2	1815	Silent Mutation	GCC,GCT	A449A	XP_011528681.1
XM_011530380.2	1815	Silent Mutation	GCC,GCT	A445A	XP_011528682.1
XM_011530381.2	1815	Silent Mutation	GCC,GCT	A444A	XP_011528683.1
XM_011530382.2	1815	Silent Mutation	GCC,GCT	A444A	XP_011528684.1
XM_011530383.2	1815	Silent Mutation	GCC,GCT	A439A	XP_011528685.1
XM_011530384.2	1815	Silent Mutation	GCC,GCT	A433A	XP_011528686.1
XM_011530386.2	1815	Silent Mutation	GCC,GCT	A268A	XP_011528688.1
XM_011530387.2	1815	Silent Mutation	GCC,GCT	A268A	XP_011528689.1
XM_011530388.2	1815	Silent Mutation	GCC,GCT	A256A	XP_011528690.1

Gene

SLC16A8

Gene Name

solute carrier family 16 member 8

There are no transcripts associated with this gene.

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