Product Details

SNP ID

rs147787222

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128149551 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGCCCCTAGGTCTCCTGTGGCTGG[G/T]CCTAGCCCTGTTGGGGGCTCTGCAT

Phenotype

MIM: 600181

Polymorphism

G/T, Transversion 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	122	Missense Mutation	GGC,GTC	G9V	NP_005555.2

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