Product Details

SNP ID
rs200747766
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:14695084 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATTGCTGGACAGCGCACGGAGGAG[C/G]CTGTGCAAATACAGGATGCTTGACC
Phenotype
MIM: 611811
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ZNF333 PubMed Links

Gene Details

Gene
ZNF333
Gene Name
zinc finger protein 333
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300912.1 230 Missense Mutation AGC,AGG S26R NP_001287841.1
NM_032433.2 230 Missense Mutation AGC,AGG S26R NP_115809.1
XM_005260098.3 230 UTR 5 XP_005260155.1
XM_006722924.2 230 Missense Mutation AGC,AGG S26R XP_006722987.1
XM_011528362.2 230 Missense Mutation AGC,AGG S26R XP_011526664.1
XM_011528363.2 230 UTR 5 XP_011526665.1
XM_011528365.2 230 UTR 5 XP_011526667.1
XM_011528366.2 230 UTR 5 XP_011526668.1
XM_011528367.2 230 UTR 5 XP_011526669.1
XM_011528368.2 230 UTR 5 XP_011526670.1
XM_011528369.2 230 UTR 5 XP_011526671.1
XM_011528371.2 230 Intron XP_011526673.1
XM_011528372.2 230 Intron XP_011526674.1
XM_017027367.1 230 Missense Mutation AGC,AGG S26R XP_016882856.1
XM_017027368.1 230 Intron XP_016882857.1
XM_017027369.1 230 UTR 5 XP_016882858.1
XM_017027370.1 230 UTR 5 XP_016882859.1
XM_017027371.1 230 UTR 5 XP_016882860.1

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