Product Details

SNP ID
rs145662068
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:60423756 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTGCGTGTAGGCATTCTCGTTC[C/T]ACCAATCTAAGAGATGAAGCAGAGA
Phenotype
MIM: 610835
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ICE2 PubMed Links

Gene Details

Gene
ICE2
Gene Name
interactor of little elongation complex ELL subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001018089.2 2939 Missense Mutation AGA,GGA R806G NP_001018099.1
NM_001276385.1 2939 Intron NP_001263314.1
NM_024611.5 2939 Missense Mutation AGA,GGA R943G NP_078887.2
XM_005254661.1 2939 Missense Mutation AGA,GGA R943G XP_005254718.1
XM_005254662.1 2939 Missense Mutation AGA,GGA R806G XP_005254719.1
XM_011522009.1 2939 Missense Mutation AGA,GGA R943G XP_011520311.1
XM_011522010.1 2939 Missense Mutation AGA,GGA R806G XP_011520312.1
XM_011522011.2 2939 Missense Mutation AGA,GGA R806G XP_011520313.1
XM_017022569.1 2939 Missense Mutation AGA,GGA R943G XP_016878058.1

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