Product Details

SNP ID
rs202211864
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:86245274 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGACTGCGCCGGCGGGAACAGACAT[G/T]CCTGCGGCCAAGAAGCAGAAGCTGA
Phenotype
MIM: 605984
Polymorphism
G/T, 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_001308007.1 731 Missense Mutation ATG,ATT M15I NP_001294936.1
NM_003797.4 731 Missense Mutation ATG,ATT M15I NP_003788.2
XM_005274373.2 731 Missense Mutation ATG,ATT M15I XP_005274430.1
XM_011545330.1 731 Missense Mutation ATG,ATT M15I XP_011543632.1
XM_011545331.1 731 Missense Mutation ATG,ATT M15I XP_011543633.1
XM_017018512.1 731 Missense Mutation ATG,ATT M15I XP_016874001.1
XM_017018513.1 731 Missense Mutation ATG,ATT M15I XP_016874002.1

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