Product Details

SNP ID

rs17851676

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:98282365 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGCCCACAGGGATACCCACCCAC[C/T]ATCCCAGGGTCTACAACATCCACAG

Phenotype

MIM: 611877 MIM: 615628

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

BAIAP2L1 PubMed Links

Additional Information

For this assay, SNP(s) [rs147351220] 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

BAIAP2L1

Gene Name

BAI1 associated protein 2 like 1

There are no transcripts associated with this gene.

Gene

BRI3

Gene Name

brain protein I3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159491.1	280	Missense Mutation	CAT,TAT	H53Y	NP_001152963.1
NM_015379.4	280	Intron			NP_056194.1
XM_017011931.1	280	Missense Mutation	CCA,CTA	P66L	XP_016867420.1
XM_017011932.1	280	Missense Mutation	CCA,CTA	P66L	XP_016867421.1
XM_017011933.1	280	Missense Mutation	CCA,CTA	P66L	XP_016867422.1
XM_017011934.1	280	Missense Mutation	CCA,CTA	P66L	XP_016867423.1
XM_017011935.1	280	Missense Mutation	CCA,CTA	P66L	XP_016867424.1
XM_017011936.1	280	Missense Mutation	CAT,TAT	H53Y	XP_016867425.1

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