Product Details

SNP ID
rs35565861
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:179443448 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGGGCCAAAGGCTTCATCATATC[A/T]TTCTGGAATGCAAGTTTTGCCTAAG
Phenotype
MIM: 612344
Polymorphism
A/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 1138 Missense Mutation AAA,AAT K330N NP_001106868.1
NM_001113398.1 1138 Missense Mutation AAA,AAT K304N NP_001106869.1
NM_001282725.1 1138 Missense Mutation AAA,AAT K304N NP_001269654.1
NM_152520.4 1138 Missense Mutation AAA,AAT K406N NP_689733.3
XM_011510713.2 1138 Missense Mutation AAA,AAT K461N XP_011509015.1
XM_011510714.2 1138 Missense Mutation AAA,AAT K448N XP_011509016.1
XM_011510715.2 1138 Missense Mutation AAA,AAT K434N XP_011509017.1
XM_011510716.2 1138 Missense Mutation AAA,AAT K364N XP_011509018.1
XM_011510717.2 1138 Missense Mutation AAA,AAT K364N XP_011509019.1
XM_011510719.2 1138 Missense Mutation AAA,AAT K344N XP_011509021.1
XM_011510720.2 1138 Missense Mutation AAA,AAT K344N XP_011509022.1
XM_011510721.2 1138 Missense Mutation AAA,AAT K331N XP_011509023.1
XM_011510723.2 1138 Intron XP_011509025.1
XM_017003435.1 1138 Missense Mutation AAA,AAT K421N XP_016858924.1
XM_017003436.1 1138 Missense Mutation AAA,AAT K344N XP_016858925.1
XM_017003437.1 1138 Missense Mutation AAA,AAT K338N XP_016858926.1
XM_017003438.1 1138 Missense Mutation AAA,AAT K304N XP_016858927.1
XM_017003439.1 1138 Missense Mutation AAA,AAT K304N XP_016858928.1
XM_017003440.1 1138 Missense Mutation AAA,AAT K292N XP_016858929.1
XM_017003441.1 1138 Intron XP_016858930.1

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