Product Details

SNP ID

rs2988414

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:6741529 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTATGTTCCTAGCTTCCTTCTGAT[A/G]TAATTTCTCTTATATCTGAACTTAT

Phenotype

MIM: 605469

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

KDM4C PubMed Links

Additional Information

For this assay, SNP(s) [rs149450823] 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

KDM4C

Gene Name

lysine demethylase 4C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146695.1		Intron			NP_001140167.1
NM_001146696.1		Intron			NP_001140168.1
NM_001304339.1		Intron			NP_001291268.1
NM_001304340.1		Intron			NP_001291269.1
NM_001304341.1		Intron			NP_001291270.1
NM_015061.3		Intron			NP_055876.2
XM_006716741.2		Intron			XP_006716804.1
XM_011517811.2		Intron			XP_011516113.1
XM_011517812.2		Intron			XP_011516114.2
XM_011517816.2		Intron			XP_011516118.1
XM_017014498.1		Intron			XP_016869987.1
XM_017014499.1		Intron			XP_016869988.1
XM_017014500.1		Intron			XP_016869989.1
XM_017014501.1		Intron			XP_016869990.1
XM_017014502.1		Intron			XP_016869991.1
XM_017014503.1		Intron			XP_016869992.1
XM_017014504.1		Intron			XP_016869993.1
XM_017014505.1		Intron			XP_016869994.1
XM_017014506.1		Intron			XP_016869995.1

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