Product Details

SNP ID
rs143260001
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:150220752 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGTTTCCTCTTCTCCCCTCGAAGA[C/T]CTCCTTCTTCTTAAAGAGTGGAAAG
Phenotype
MIM: 609611
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ANP32E PubMed Links

Gene Details

Gene
ANP32E
Gene Name
acidic nuclear phosphoprotein 32 family member E
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136478.3 895 Missense Mutation GAT,GGT D208G NP_001129950.1
NM_001136479.2 895 Missense Mutation GAT,GGT D201G NP_001129951.1
NM_001280559.1 895 Missense Mutation GAT,GGT D248G NP_001267488.1
NM_001280560.1 895 UTR 3 NP_001267489.1
NM_030920.4 895 Missense Mutation GAT,GGT D249G NP_112182.1
XM_005245513.3 895 Missense Mutation GAT,GGT D267G XP_005245570.1
XM_005245514.3 895 Missense Mutation ATC,GTC I231V XP_005245571.1
XM_017002418.1 895 Missense Mutation GAT,GGT D266G XP_016857907.1

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