Product Details

SNP ID

rs150975968

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128151700 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGTTGCCAGCCCGGCGAGTTCA[C/T]GCTGGGCAACATTAAGAGTGAGTCT

Phenotype

MIM: 600181

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C9orf16 PubMed Links

Gene Details

Gene

C9orf16

Gene Name

chromosome 9 open reading frame 16

There are no transcripts associated with this gene.

Gene

LCN2

Gene Name

lipocalin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005564.4	434	Missense Mutation	ACG,ATG	T113M	NP_005555.2

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