Product Details

SNP ID
rs199943809
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:86245285 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGAACAGACATGCCTGCGGCCA[A/G]GAAGCAGAAGCTGAGCAGTGACGAG
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_001308007.1 742 Missense Mutation AAG,AGG K19R NP_001294936.1
NM_003797.4 742 Missense Mutation AAG,AGG K19R NP_003788.2
XM_005274373.2 742 Missense Mutation AAG,AGG K19R XP_005274430.1
XM_011545330.1 742 Missense Mutation AAG,AGG K19R XP_011543632.1
XM_011545331.1 742 Missense Mutation AAG,AGG K19R XP_011543633.1
XM_017018512.1 742 Missense Mutation AAG,AGG K19R XP_016874001.1
XM_017018513.1 742 Missense Mutation AAG,AGG K19R XP_016874002.1

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