Product Details

SNP ID
rs151272775
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:50294948 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTTCCAAGAAGATAAACAGGAACA[C/T]ACATGCTCTTGGACTGGCCAAAAAG
Phenotype
MIM: 300456
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CCNB3 PubMed Links

Gene Details

Gene
CCNB3
Gene Name
cyclin B3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033031.2 588 Missense Mutation ACA,ATA T97I NP_149020.2
NM_033670.2 588 Intron NP_391990.1
XM_017029913.1 588 Missense Mutation ACA,ATA T97I XP_016885402.1
XM_017029914.1 588 Missense Mutation ACA,ATA T97I XP_016885403.1
XM_017029915.1 588 Missense Mutation ACA,ATA T97I XP_016885404.1
XM_017029916.1 588 Missense Mutation ACA,ATA T97I XP_016885405.1
XM_017029917.1 588 Missense Mutation ACA,ATA T97I XP_016885406.1
XM_017029918.1 588 Missense Mutation ACA,ATA T97I XP_016885407.1

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