Product Details

SNP ID: rs139697290
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:67842951 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCAGCAGCAGCAGCAGCAGCAGCAG[C/T]CCTCACCCTCTGCCTCCACTGCCCA
Phenotype: MIM: 611510 MIM: 605813 MIM: 609119
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CENPT PubMed Links

Gene Details

Gene: CENPT
Gene Name: centromere protein T

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025082.3	642	Intron			NP_079358.3
XM_006721277.2	642	Intron			XP_006721340.1
XM_011523344.1	642	Intron			XP_011521646.1
XM_011523345.1	642	Intron			XP_011521647.1
XM_017023712.1	642	Intron			XP_016879201.1
XM_017023713.1	642	Intron			XP_016879202.1
XM_017023714.1	642	Intron			XP_016879203.1
XM_017023715.1	642	Intron			XP_016879204.1
XM_017023716.1	642	Intron			XP_016879205.1
XM_017023717.1	642	Intron			XP_016879206.1

Gene: NUTF2
Gene Name: nuclear transport factor 2

There are no transcripts associated with this gene.

Gene: THAP11
Gene Name: THAP domain containing 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020457.2	642	Missense Mutation	CCC,TCC	P133S	NP_065190.2

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