Product Details

SNP ID
rs201857174
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:167687650 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTATTGATATTTCTTGAAGACAT[C/T]ATTCACTGTATCAAGAAGTTCTTTT
Phenotype
MIM: 609118
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PDCD10 PubMed Links

Gene Details

Gene
PDCD10
Gene Name
programmed cell death 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007217.3 1568 Missense Mutation AAT,GAT N147D NP_009148.2
NM_145859.1 1568 Intron NP_665858.1
NM_145860.1 1568 Intron NP_665859.1
XM_005247086.4 1568 Missense Mutation AAT,GAT N147D XP_005247143.1
XM_005247087.4 1568 Missense Mutation AAT,GAT N147D XP_005247144.1
XM_005247088.3 1568 Missense Mutation AAT,GAT N147D XP_005247145.1
XM_006713485.3 1568 Missense Mutation AAT,GAT N147D XP_006713548.1
XM_011512368.2 1568 Missense Mutation AAT,GAT N147D XP_011510670.1
XM_011512369.2 1568 Missense Mutation AAT,GAT N147D XP_011510671.1
XM_017005644.1 1568 Missense Mutation AAT,GAT N147D XP_016861133.1
XM_017005645.1 1568 Missense Mutation AAT,GAT N84D XP_016861134.1

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