Product Details

SNP ID
rs58602893
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:47191850 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGACGAAGCAGTAGATAGTAGTCT[C/G]TGTTATAGAGTTGCTGGAGAGAAGG
Phenotype
MIM: 609295
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SEMA6D PubMed Links

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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