Product Details

SNP ID

rs16886496

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:56921702 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTGAAGCAACTTATACTTACAAA[C/T]ATTAGCAATGCAGCCAAACATTTGT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MIER3 PubMed Links

Gene Details

Gene

MIER3

Gene Name

MIER family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001297598.1	3142	UTR 3			NP_001284527.1
NM_001297599.1	3142	UTR 3			NP_001284528.1
NM_152622.4	3142	UTR 3			NP_689835.3
XM_011543216.1	3142	UTR 3			XP_011541518.1
XM_011543217.1	3142	UTR 3			XP_011541519.1
XM_017009149.1	3142	UTR 3			XP_016864638.1

Gene

SETD9

Gene Name

SET domain containing 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171990.2	3142	Intron			NP_001165461.1
NM_001323018.1	3142	Intron			NP_001309947.1
NM_001323019.1	3142	Intron			NP_001309948.1
NM_001323020.1	3142	Intron			NP_001309949.1
NM_001323022.1	3142	Intron			NP_001309951.1
NM_153706.3	3142	Intron			NP_714917.2
XM_005248426.4	3142	Intron			XP_005248483.1
XM_011543139.2	3142	Intron			XP_011541441.1
XM_011543140.2	3142	Intron			XP_011541442.1

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