Product Details

SNP ID
rs1894608
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:29207270 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAGACAGGGGTGGACGTGTGGCA[A/G]ATGTTACAGCCACCACCTATTGTGT
Phenotype
MIM: 608926
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
EMID1 PubMed Links

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 1037 Intron NP_001254824.1
NM_133455.3 1037 Intron NP_597712.2
XM_005261328.2 1037 Intron XP_005261385.1
XM_005261329.2 1037 Intron XP_005261386.1
XM_011529868.2 1037 Intron XP_011528170.1
XM_011529869.2 1037 Intron XP_011528171.1
XM_011529870.2 1037 Intron XP_011528172.1
XM_011529871.2 1037 Intron XP_011528173.1
XM_011529872.2 1037 Intron XP_011528174.1
XM_011529873.2 1037 Intron XP_011528175.1
XM_011529874.2 1037 UTR 5 XP_011528176.1
XM_011529875.2 1037 Intron XP_011528177.1
XM_011529876.1 1037 Intron XP_011528178.1
XM_017028589.1 1037 UTR 5 XP_016884078.1

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