Product Details

SNP ID

rs140444141

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:135663387 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCCCAGGAGTTCGATCCCCACAC[C/T]GTTATGCAGAGGAACTACAACGTGG

Phenotype

MIM: 612903

Polymorphism

C/T, 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	66	Silent Mutation	ACC,ACT	T22T	NP_001001676.1
XM_017014712.1	66	Silent Mutation	ACC,ACT	T22T	XP_016870201.1

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