Product Details

SNP ID

rs2835341

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:36393837 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAATTTTGGAATCTCATTTTAATGC[G/T]TAGTTCTGGAGATTGTCCTTATATT

Phenotype

MIM: 601245

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CHAF1B PubMed Links

Additional Information

For this assay, SNP(s) [rs114109249] 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

CHAF1B

Gene Name

chromatin assembly factor 1 subunit B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005441.2		Intron			NP_005432.1
XM_011529755.2		Intron			XP_011528057.1
XM_017028477.1		Intron			XP_016883966.1
XM_017028478.1		Intron			XP_016883967.1

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