Product Details

SNP ID

rs138644874

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51125367 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGGAAGTATAAAATGGAATTATAA[A/C]CATCACCGGCTCTCTGTGAATGTGA

Phenotype

MIM: 605640

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SIGLEC9 PubMed Links

Additional Information

For this assay, SNP(s) [rs16988910] are located under a probe and SNP(s) [rs2075803] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SIGLEC9

Gene Name

sialic acid binding Ig like lectin 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198558.1	460	Missense Mutation	AAA,AAC	K131N	NP_001185487.1
NM_014441.2	460	Missense Mutation	AAA,AAC	K131N	NP_055256.1
XM_006723146.3	460	Missense Mutation	AAA,AAC	K131N	XP_006723209.1
XM_011526730.2	460	Missense Mutation	AAA,AAC	K131N	XP_011525032.1
XM_011526732.2	460	Missense Mutation	AAA,AAC	K131N	XP_011525034.1
XM_017026595.1	460	Missense Mutation	AAA,AAC	K131N	XP_016882084.1
XM_017026596.1	460	Missense Mutation	AAA,AAC	K131N	XP_016882085.1

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