Product Details

SNP ID
rs200782451
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:86245272 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCGACTGCGCCGGCGGGAACAGAC[A/G]TGCCTGCGGCCAAGAAGCAGAAGCT
Phenotype
MIM: 605984
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EED PubMed Links

Gene Details

Gene
EED
Gene Name
embryonic ectoderm development
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308007.1 729 Missense Mutation ATG,GTG M15V NP_001294936.1
NM_003797.4 729 Missense Mutation ATG,GTG M15V NP_003788.2
XM_005274373.2 729 Missense Mutation ATG,GTG M15V XP_005274430.1
XM_011545330.1 729 Missense Mutation ATG,GTG M15V XP_011543632.1
XM_011545331.1 729 Missense Mutation ATG,GTG M15V XP_011543633.1
XM_017018512.1 729 Missense Mutation ATG,GTG M15V XP_016874001.1
XM_017018513.1 729 Missense Mutation ATG,GTG M15V XP_016874002.1

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