Product Details

SNP ID
rs201711487
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:160565622 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAGCATGAGTCATCCCTCATGCAC[G/T]CCGTGCCACATCTCTGTTCGTGGAG
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
ATP10B PubMed Links

Gene Details

Gene
ATP10B
Gene Name
ATPase phospholipid transporting 10B (putative)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025153.2 4621 Missense Mutation GAG,GCG E1406A NP_079429.2
XM_006714833.2 4621 Missense Mutation GAG,GCG E1406A XP_006714896.1
XM_011534468.2 4621 Missense Mutation GAG,GCG E1406A XP_011532770.1
XM_011534469.1 4621 Missense Mutation GAG,GCG E1406A XP_011532771.1
XM_011534472.2 4621 Missense Mutation GAG,GCG E1378A XP_011532774.1
XM_017009252.1 4621 Missense Mutation GAG,GCG E1394A XP_016864741.1
XM_017009253.1 4621 Missense Mutation GAG,GCG E1339A XP_016864742.1

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