Product Details

SNP ID

rs142490331

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51414864 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGATCCACTCTGGGCCCCATGGAC[A/G]TTCCAGGCCTCACAGCGGAGCCTGA

Phenotype

MIM: 606091

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LOC100129083 PubMed Links

Additional Information

For this assay, SNP(s) [rs3810099] are located under a probe and SNP(s) [rs1833785] 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

LOC100129083

Gene Name

uncharacterized LOC100129083

There are no transcripts associated with this gene.

Gene

SIGLEC10

Gene Name

sialic acid binding Ig like lectin 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171156.1	1797	Silent Mutation			NP_001164627.1
NM_001171157.1	1797	Intron			NP_001164628.1
NM_001171158.1	1797	Intron			NP_001164629.1
NM_001171159.1	1797	Intron			NP_001164630.1
NM_001171161.1	1797	Intron			NP_001164632.1
NM_001322105.1	1797	Intron			NP_001309034.1
NM_033130.4	1797	Silent Mutation			NP_149121.2
XM_005259366.4	1797	Silent Mutation			XP_005259423.1
XM_005259367.3	1797	Silent Mutation			XP_005259424.1
XM_011527439.1	1797	Silent Mutation			XP_011525741.1

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