Product Details

SNP ID
rs112589121
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:149765292 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCCGGTCCGCCAGGCGCGCTGG[C/T]CAGGGGCTTGGCGGCGGGGGCATCC
Phenotype
MIM: 614040
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ZNF467 PubMed Links

Gene Details

Gene
ZNF467
Gene Name
zinc finger protein 467
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005249959.4 1323 Missense Mutation ACC,GCC T404A XP_005250016.1
XM_005249960.4 1323 Missense Mutation ACC,GCC T404A XP_005250017.1
XM_005249961.4 1323 Missense Mutation ACC,GCC T404A XP_005250018.1
XM_006715864.3 1323 Missense Mutation ACC,GCC T445A XP_006715927.1
XM_011515855.2 1323 Missense Mutation ACC,GCC T655A XP_011514157.1
XM_011515856.2 1323 Missense Mutation ACC,GCC T655A XP_011514158.1
XM_011515857.2 1323 Missense Mutation ACC,GCC T618A XP_011514159.1
XM_011515858.1 1323 Missense Mutation ACC,GCC T404A XP_011514160.1
XM_017011799.1 1323 Missense Mutation ACC,GCC T579A XP_016867288.1

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