Product Details

SNP ID

rs2457774

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:21810492 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCCCACATCCAACACTGAAGATTA[C/T]ACTGCAGCATGAGGTTTGGAAACAT

Phenotype

MIM: 603972

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ZNF43 PubMed Links

Additional Information

For this assay, SNP(s) [rs2457773] are located under a probe 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

ZNF43

Gene Name

zinc finger protein 43

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256648.1		Intron			NP_001243577.1
NM_001256649.1		Intron			NP_001243578.1
NM_001256650.1		Intron			NP_001243579.1
NM_001256651.1		Intron			NP_001243580.1
NM_001256653.1		Intron			NP_001243582.1
NM_001256654.1		Intron			NP_001243583.1
NM_003423.3		Intron			NP_003414.2
XM_011528257.2		Intron			XP_011526559.1
XM_011528259.2		Intron			XP_011526561.1
XM_017027207.1		Intron			XP_016882696.1
XM_017027208.1		Intron			XP_016882697.1
XM_017027209.1		Intron			XP_016882698.1
XM_017027210.1		Intron			XP_016882699.1
XM_017027211.1		Intron			XP_016882700.1
XM_017027212.1		Intron			XP_016882701.1
XM_017027213.1		Intron			XP_016882702.1
XM_017027214.1		Intron			XP_016882703.1
XM_017027215.1		Intron			XP_016882704.1
XM_017027216.1		Intron			XP_016882705.1

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