Product Details

SNP ID

rs148878394

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:180911370 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCAGTTCCTCTCATTTCCATCAC[A/G]GGATATGTTGATAGAGACATCCAGC

Phenotype

MIM: 615606

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

BTNL8 PubMed Links

Additional Information

For this assay, SNP(s) [rs2276995] 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

BTNL8

Gene Name

butyrophilin like 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040462.2	468	Silent Mutation	ACA,ACG	T143T	NP_001035552.1
NM_001159707.1	468	Silent Mutation	ACA,ACG	T27T	NP_001153179.1
NM_001159708.1	468	Silent Mutation	ACA,ACG	T143T	NP_001153180.1
NM_001159709.1	468	Silent Mutation	ACA,ACG	T18T	NP_001153181.1
NM_001159710.1	468	UTR 5			NP_001153182.1
NM_024850.2	468	Silent Mutation	ACA,ACG	T143T	NP_079126.1
XM_011534649.1	468	Silent Mutation	ACA,ACG	T143T	XP_011532951.1
XM_011534650.2	468	Silent Mutation	ACA,ACG	T93T	XP_011532952.1
XM_011534651.2	468	Silent Mutation	ACA,ACG	T32T	XP_011532953.1
XM_011534652.2	468	Silent Mutation	ACA,ACG	T24T	XP_011532954.1
XM_011534653.2	468	Intron			XP_011532955.1

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