Product Details

SNP ID
rs104894481
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:44711577 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGCTCCGTGGCCTTAGCTGTGCTC[C/G]CGCTACTCTCTCTTTCTGGCCTGGA
Phenotype
MIM: 109700 MIM: 614661
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
B2M PubMed Links

Gene Details

Gene
B2M
Gene Name
beta-2-microglobulin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004048.2 86 Missense Mutation CCG,GCG P11A NP_004039.1
XM_005254549.3 86 Missense Mutation CCG,GCG P11A XP_005254606.1
Gene
PATL2
Gene Name
PAT1 homolog 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145112.1 86 Intron NP_001138584.1
XM_011521336.2 86 Intron XP_011519638.2
XM_011521337.2 86 Intron XP_011519639.2
XM_011521338.2 86 Intron XP_011519640.1
XM_011521339.2 86 Intron XP_011519641.1
XM_011521340.2 86 Intron XP_011519642.1
XM_011521341.1 86 Intron XP_011519643.1
XM_011521342.2 86 Intron XP_011519644.1
XM_011521343.2 86 Intron XP_011519645.1
XM_011521344.2 86 Intron XP_011519646.1
XM_011521345.2 86 Intron XP_011519647.1
XM_011521346.2 86 Intron XP_011519648.2
XM_011521347.1 86 Intron XP_011519649.1
XM_011521348.2 86 Intron XP_011519650.1
XM_017022000.1 86 Intron XP_016877489.1
XM_017022001.1 86 Intron XP_016877490.1

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