Product Details

SNP ID
rs200506006
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:86245260 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGAGAGGGAAGTGTCGACTGCGCCG[C/G]CGGGAACAGACATGCCTGCGGCCAA
Phenotype
MIM: 605984
Polymorphism
C/G, Transversion 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_001308007.1 717 Missense Mutation CCG,GCG P11A NP_001294936.1
NM_003797.4 717 Missense Mutation CCG,GCG P11A NP_003788.2
XM_005274373.2 717 Missense Mutation CCG,GCG P11A XP_005274430.1
XM_011545330.1 717 Missense Mutation CCG,GCG P11A XP_011543632.1
XM_011545331.1 717 Missense Mutation CCG,GCG P11A XP_011543633.1
XM_017018512.1 717 Missense Mutation CCG,GCG P11A XP_016874001.1
XM_017018513.1 717 Missense Mutation CCG,GCG P11A XP_016874002.1

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