Product Details

SNP ID

rs12628475

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:29210918 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGTGAGAAGATGGCCAACAGTACC[C/T]TGCTGGGCCTGCCTTCACCTGTTTG

Phenotype

MIM: 608926

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EMID1 PubMed Links

Additional Information

For this assay, SNP(s) [rs142157348] 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

EMID1

Gene Name

EMI domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001267895.1		Intron			NP_001254824.1
NM_133455.3		Intron			NP_597712.2
XM_005261328.2		Intron			XP_005261385.1
XM_005261329.2		Intron			XP_005261386.1
XM_011529868.2		Intron			XP_011528170.1
XM_011529869.2		Intron			XP_011528171.1
XM_011529870.2		Intron			XP_011528172.1
XM_011529871.2		Intron			XP_011528173.1
XM_011529872.2		Intron			XP_011528174.1
XM_011529873.2		Intron			XP_011528175.1
XM_011529874.2		Intron			XP_011528176.1
XM_011529875.2		Intron			XP_011528177.1
XM_011529876.1		Intron			XP_011528178.1
XM_017028589.1		Intron			XP_016884078.1

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