Product Details

SNP ID

rs200277241

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:135664247 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGGAGACCTGAGGGTCTTCGTCC[A/G]GAATATTGAACACTTGAAGAACGGC

Phenotype

MIM: 612903

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LCN9 PubMed Links

Gene Details

Gene

LCN9

Gene Name

lipocalin 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001676.1	182	Missense Mutation	CAG,CGG	Q61R	NP_001001676.1
XM_017014712.1	182	Missense Mutation	CAG,CGG	Q61R	XP_016870201.1

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