Product Details

SNP ID
rs145674802
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:86245318 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGCTGAGCAGTGACGAGAACAGCA[A/T]TCCAGACCTCTCTGGAGACGAGAAT
Phenotype
MIM: 605984
Polymorphism
A/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_001308007.1 775 Missense Mutation AAT,ATT N30I NP_001294936.1
NM_003797.4 775 Missense Mutation AAT,ATT N30I NP_003788.2
XM_005274373.2 775 Missense Mutation AAT,ATT N30I XP_005274430.1
XM_011545330.1 775 Missense Mutation AAT,ATT N30I XP_011543632.1
XM_011545331.1 775 Missense Mutation AAT,ATT N30I XP_011543633.1
XM_017018512.1 775 Missense Mutation AAT,ATT N30I XP_016874001.1
XM_017018513.1 775 Missense Mutation AAT,ATT N30I XP_016874002.1

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