Product Details

SNP ID
rs1501466
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:2299654 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGCGGTGGCAGGTGGAACAAGGGC[A/G]CCATGGGCGGAGGGTTGGGCAGCTG
Phenotype
MIM: 611033 MIM: 603853
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C11orf21 PubMed Links

Gene Details

Gene
C11orf21
Gene Name
chromosome 11 open reading frame 21
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_011520034.1 391 Silent Mutation GGC,GGT G113G XP_011518336.1
Gene
TSPAN32
Gene Name
tetraspanin 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_139022.2 391 Intron NP_620591.3
XM_005252719.4 391 Intron XP_005252776.1
XM_005252720.4 391 Intron XP_005252777.1
XM_011519815.2 391 Intron XP_011518117.2
XM_011519818.2 391 Intron XP_011518120.2
XM_011519819.1 391 Intron XP_011518121.1
XM_011519822.1 391 Intron XP_011518124.1
XM_011519828.2 391 Intron XP_011518130.1
XM_011519829.2 391 Intron XP_011518131.2
XM_017017064.1 391 Intron XP_016872553.1
XM_017017065.1 391 Intron XP_016872554.1
XM_017017066.1 391 Intron XP_016872555.1
XM_017017067.1 391 Intron XP_016872556.1
XM_017017068.1 391 Intron XP_016872557.1
XM_017017069.1 391 Intron XP_016872558.1
XM_017017070.1 391 Intron XP_016872559.1
XM_017017071.1 391 Intron XP_016872560.1

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