Product Details

SNP ID
rs74635000
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:167695602 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAACAAATAATTGCTTACTTGATT[A/G]TCTGCAGAAACCTCACTCTGTCATT
Phenotype
MIM: 609118
Polymorphism
A/G, 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 1518 Missense Mutation ACA,ATA T130I NP_009148.2
NM_145859.1 1518 Intron NP_665858.1
NM_145860.1 1518 Intron NP_665859.1
XM_005247086.4 1518 Missense Mutation ACA,ATA T130I XP_005247143.1
XM_005247087.4 1518 Missense Mutation ACA,ATA T130I XP_005247144.1
XM_005247088.3 1518 Missense Mutation ACA,ATA T130I XP_005247145.1
XM_006713485.3 1518 Missense Mutation ACA,ATA T130I XP_006713548.1
XM_011512368.2 1518 Missense Mutation ACA,ATA T130I XP_011510670.1
XM_011512369.2 1518 Missense Mutation ACA,ATA T130I XP_011510671.1
XM_017005644.1 1518 Missense Mutation ACA,ATA T130I XP_016861133.1
XM_017005645.1 1518 Missense Mutation ACA,ATA T67I XP_016861134.1

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