Product Details

SNP ID
rs200829573
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:133187878 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGCTCTTGAGTCCACAGGTCCCA[C/T]CTCTCCAAGAACGAAACAGTTCATG
Phenotype
MIM: 604753
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ZNF268 PubMed Links

Gene Details

Gene
ZNF268
Gene Name
zinc finger protein 268
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001165881.2 370 Missense Mutation CCT,TCT P14S NP_001159353.1
NM_001165882.2 370 UTR 5 NP_001159354.1
NM_001165883.1 370 Missense Mutation CCT,TCT P14S NP_001159355.1
NM_001165884.2 370 Intron NP_001159356.2
NM_001165885.1 370 Missense Mutation CCT,TCT P14S NP_001159357.1
NM_001165886.1 370 Intron NP_001159358.1
NM_001165887.1 370 Intron NP_001159359.1
NM_003415.2 370 Missense Mutation CCT,TCT P14S NP_003406.1
NM_152943.2 370 Missense Mutation CCT,TCT P14S NP_694422.2

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