Product Details

SNP ID

rs1865675

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:20556742 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTCTCAAACCCATCAGTTGCTGCA[C/T]TTTAGTTTAAATTGTACATATTTGG

Phenotype

MIM: 609359

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HS1BP3 PubMed Links

Additional Information

For this assay, SNP(s) [rs113153958] 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

HS1BP3

Gene Name

HCLS1 binding protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022460.3	2594	Intron			NP_071905.3
XM_017004696.1	2594	UTR 3			XP_016860185.1
XM_017004697.1	2594	UTR 3			XP_016860186.1
XM_017004698.1	2594	Intron			XP_016860187.1
XM_017004699.1	2594	UTR 3			XP_016860188.1
XM_017004700.1	2594	Intron			XP_016860189.1
XM_017004701.1	2594	Intron			XP_016860190.1

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