Product Details

SNP ID
rs3194380
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:149765644 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATGGATGCGCTGGTGCCGAATCAA[G/T]TGCGTCTTCTTGCGAAAGCGCTTCT
Phenotype
MIM: 614040
Polymorphism
G/T, Transversion 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_005249959.4 971 Missense Mutation CAA,CAC Q286H XP_005250016.1
XM_005249960.4 971 Missense Mutation CAA,CAC Q286H XP_005250017.1
XM_005249961.4 971 Missense Mutation CAA,CAC Q286H XP_005250018.1
XM_006715864.3 971 Missense Mutation CAA,CAC Q327H XP_006715927.1
XM_011515855.2 971 Missense Mutation CAA,CAC Q537H XP_011514157.1
XM_011515856.2 971 Missense Mutation CAA,CAC Q537H XP_011514158.1
XM_011515857.2 971 Missense Mutation CAA,CAC Q500H XP_011514159.1
XM_011515858.1 971 Missense Mutation CAA,CAC Q286H XP_011514160.1
XM_017011799.1 971 Missense Mutation CAA,CAC Q461H XP_016867288.1

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