Product Details

SNP ID

rs28532071

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:47193981 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTGAAACAAGGATAATGTCTGTT[G/T]TGATTACATTTGTTCCCTTAATACT

Phenotype

MIM: 609295

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SEMA6D PubMed Links

Additional Information

For this assay, SNP(s) [rs201559354] 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

SEMA6D

Gene Name

semaphorin 6D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198999.1		Intron			NP_001185928.1
NM_020858.1		Intron			NP_065909.1
NM_024966.2		Intron			NP_079242.2
NM_153616.1		Intron			NP_705869.1
NM_153617.1		Intron			NP_705870.1
NM_153618.1		Intron			NP_705871.1
NM_153619.1		Intron			NP_705872.1
XM_005254685.3		Intron			XP_005254742.1
XM_005254686.2		Intron			XP_005254743.1
XM_005254687.2		Intron			XP_005254744.1
XM_005254689.3		Intron			XP_005254746.1
XM_011522075.2		Intron			XP_011520377.1
XM_011522076.2		Intron			XP_011520378.1
XM_011522077.2		Intron			XP_011520379.1
XM_011522078.2		Intron			XP_011520380.1
XM_011522079.2		Intron			XP_011520381.1
XM_011522080.2		Intron			XP_011520382.1
XM_011522081.2		Intron			XP_011520383.1
XM_017022617.1		Intron			XP_016878106.1
XM_017022618.1		Intron			XP_016878107.1
XM_017022619.1		Intron			XP_016878108.1
XM_017022620.1		Intron			XP_016878109.1
XM_017022621.1		Intron			XP_016878110.1
XM_017022622.1		Intron			XP_016878111.1

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