Product Details

SNP ID
rs11548975
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:149764904 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGAGCCTGTGTGGATCGCCTGG[C/T]GGCGGACTAGGTTGGTTTTGGAGCT
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 1711 Missense Mutation XP_005250016.1
XM_005249960.4 1711 Missense Mutation XP_005250017.1
XM_005249961.4 1711 Missense Mutation XP_005250018.1
XM_006715864.3 1711 Missense Mutation XP_006715927.1
XM_011515855.2 1711 Missense Mutation XP_011514157.1
XM_011515856.2 1711 Missense Mutation XP_011514158.1
XM_011515857.2 1711 Missense Mutation XP_011514159.1
XM_011515858.1 1711 Missense Mutation XP_011514160.1
XM_017011799.1 1711 Missense Mutation XP_016867288.1

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