Product Details

SNP ID

rs10775668

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:41306102 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCATCTCAAGAAACCACCCATTTCA[C/T]TCAATCATAAGAAGCAATTCCTCAT

Phenotype

MIM: 608617

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM3B PubMed Links

Additional Information

For this assay, SNP(s) [rs115287974] 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

FAM3B

Gene Name

family with sequence similarity 3 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_058186.3		Intron			NP_478066.3
NM_206964.1		Intron			NP_996847.1
XM_011529648.2		Intron			XP_011527950.2
XM_011529649.2		Intron			XP_011527951.1

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