Product Details

SNP ID

rs2835239

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.21:36038179 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGAAGCACAGCATTAGTCTCTTCTA[C/T]GAAATAATAGCATATTTTCTGGGCT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SETD4 PubMed Links

Gene Details

Gene

SETD4

Gene Name

SET domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007259.2	1366	Intron			NP_001007260.1
NM_001007261.2	1366	Intron			NP_001007262.1
NM_001286752.1	1366	Missense Mutation	ATA,GTA	I363V	NP_001273681.1
NM_017438.4	1366	Missense Mutation	ATA,GTA	I387V	NP_059134.1
XM_011529636.1	1366	Missense Mutation	ATA,GTA	I387V	XP_011527938.1
XM_011529637.1	1366	Missense Mutation	ATA,GTA	I387V	XP_011527939.1
XM_011529638.2	1366	Missense Mutation	ATA,GTA	I387V	XP_011527940.1
XM_011529639.1	1366	Missense Mutation	ATA,GTA	I387V	XP_011527941.1
XM_011529640.2	1366	Missense Mutation	ATA,GTA	I387V	XP_011527942.1
XM_011529642.1	1366	Missense Mutation	ATA,GTA	I363V	XP_011527944.1
XM_011529643.1	1366	Missense Mutation	ATA,GTA	I363V	XP_011527945.1
XM_011529644.1	1366	Missense Mutation	ATA,GTA	I363V	XP_011527946.1
XM_017028403.1	1366	Missense Mutation	ATA,GTA	I387V	XP_016883892.1
XM_017028404.1	1366	Missense Mutation	ATA,GTA	I363V	XP_016883893.1
XM_017028405.1	1366	Intron			XP_016883894.1

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