Product Details

SNP ID
rs139088194
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:27550373 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAATAAGCAGGAGTTCCCAAGACAA[C/T]AGTTTTAATGAAAAAAGGCTGATTG
Phenotype
MIM: 609733
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LNX2 PubMed Links

Gene Details

Gene
LNX2
Gene Name
ligand of numb-protein X 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153371.3 2065 Missense Mutation ATT,GTT I633V NP_699202.1
XM_011534995.2 2065 Missense Mutation ATT,GTT I510V XP_011533297.1
XM_017020434.1 2065 Missense Mutation ATT,GTT I633V XP_016875923.1

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