Product Details

SNP ID
rs145072775
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:179443441 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAAGGCTGGGGCCAAAGGCTTCA[G/T]CATATCTTTCTGGAATGCAAGTTTT
Phenotype
MIM: 612344
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ZNF385B PubMed Links

Gene Details

Gene
ZNF385B
Gene Name
zinc finger protein 385B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001113397.1 1145 Missense Mutation NP_001106868.1
NM_001113398.1 1145 Missense Mutation NP_001106869.1
NM_001282725.1 1145 Missense Mutation NP_001269654.1
NM_152520.4 1145 Missense Mutation NP_689733.3
XM_011510713.2 1145 Missense Mutation XP_011509015.1
XM_011510714.2 1145 Missense Mutation XP_011509016.1
XM_011510715.2 1145 Missense Mutation XP_011509017.1
XM_011510716.2 1145 Missense Mutation XP_011509018.1
XM_011510717.2 1145 Missense Mutation XP_011509019.1
XM_011510719.2 1145 Missense Mutation XP_011509021.1
XM_011510720.2 1145 Missense Mutation XP_011509022.1
XM_011510721.2 1145 Missense Mutation XP_011509023.1
XM_011510723.2 1145 Intron XP_011509025.1
XM_017003435.1 1145 Missense Mutation XP_016858924.1
XM_017003436.1 1145 Missense Mutation XP_016858925.1
XM_017003437.1 1145 Missense Mutation XP_016858926.1
XM_017003438.1 1145 Missense Mutation XP_016858927.1
XM_017003439.1 1145 Missense Mutation XP_016858928.1
XM_017003440.1 1145 Missense Mutation XP_016858929.1
XM_017003441.1 1145 Intron XP_016858930.1

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