Product Details

SNP ID

rs7991203

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:27546403 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCATGTCAATTAGAATATCAAAG[C/G]ATTTCAAAATCAAACTGCTTCCAAA

Phenotype

MIM: 609733

Polymorphism

C/G, Transversion 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	4173	UTR 3			NP_699202.1
XM_011534995.2	4173	UTR 3			XP_011533297.1
XM_017020434.1	4173	UTR 3			XP_016875923.1

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