Product Details

SNP ID

rs273641

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51252410 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAAAGAAGAAATCAGAATTTTGTA[C/G]TTAAATGGATCATTACATCTCCAGC

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SIGLECL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs78561654] 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

SIGLECL1

Gene Name

SIGLEC family like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308437.1		Intron			NP_001295366.1
NM_173635.2		Intron			NP_775906.1
XM_005258799.4		Intron			XP_005258856.1
XM_011526821.2		Intron			XP_011525123.1
XM_017026647.1		Intron			XP_016882136.1

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