Product Details

SNP ID
rs191414187
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:14695101 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGAGGAGCCTGTGCAAATACAGGA[G/T]GCTTGACCAGTGCAGGACCCTGGCC
Phenotype
MIM: 611811
Polymorphism
G/T, 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_001300912.1 247 Missense Mutation AGG,ATG R32M NP_001287841.1
NM_032433.2 247 Missense Mutation AGG,ATG R32M NP_115809.1
XM_005260098.3 247 UTR 5 XP_005260155.1
XM_006722924.2 247 Missense Mutation AGG,ATG R32M XP_006722987.1
XM_011528362.2 247 Missense Mutation AGG,ATG R32M XP_011526664.1
XM_011528363.2 247 UTR 5 XP_011526665.1
XM_011528365.2 247 UTR 5 XP_011526667.1
XM_011528366.2 247 UTR 5 XP_011526668.1
XM_011528367.2 247 UTR 5 XP_011526669.1
XM_011528368.2 247 UTR 5 XP_011526670.1
XM_011528369.2 247 UTR 5 XP_011526671.1
XM_011528371.2 247 Intron XP_011526673.1
XM_011528372.2 247 Intron XP_011526674.1
XM_017027367.1 247 Missense Mutation AGG,ATG R32M XP_016882856.1
XM_017027368.1 247 Intron XP_016882857.1
XM_017027369.1 247 UTR 5 XP_016882858.1
XM_017027370.1 247 UTR 5 XP_016882859.1
XM_017027371.1 247 UTR 5 XP_016882860.1

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