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AGAGCAGAGCCAAAGGCAACAGAAC[C/G]AGGGATTCTCCGTGCCACAGGTGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611811 | ||||||||||||||||||||
Literature Links: |
ZNF333 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ZNF333 - zinc finger protein 333 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300912.1 | 349 | Missense Mutation | CCA,CGA | P,R 66 | NP_001287841.1 | |
NM_032433.2 | 349 | Missense Mutation | CCA,CGA | P,R 66 | NP_115809.1 | |
XM_005260098.3 | 349 | UTR 5 | XP_005260155.1 | |||
XM_006722924.2 | 349 | Missense Mutation | CCA,CGA | P,R 66 | XP_006722987.1 | |
XM_011528362.2 | 349 | Missense Mutation | CCA,CGA | P,R 66 | XP_011526664.1 | |
XM_011528363.2 | 349 | UTR 5 | XP_011526665.1 | |||
XM_011528365.2 | 349 | UTR 5 | XP_011526667.1 | |||
XM_011528366.2 | 349 | UTR 5 | XP_011526668.1 | |||
XM_011528367.2 | 349 | UTR 5 | XP_011526669.1 | |||
XM_011528368.2 | 349 | UTR 5 | XP_011526670.1 | |||
XM_011528369.2 | 349 | UTR 5 | XP_011526671.1 | |||
XM_011528371.2 | 349 | Intron | XP_011526673.1 | |||
XM_011528372.2 | 349 | Intron | XP_011526674.1 | |||
XM_017027367.1 | 349 | Missense Mutation | CCA,CGA | P,R 66 | XP_016882856.1 | |
XM_017027368.1 | 349 | UTR 5 | XP_016882857.1 | |||
XM_017027369.1 | 349 | UTR 5 | XP_016882858.1 | |||
XM_017027370.1 | 349 | UTR 5 | XP_016882859.1 | |||
XM_017027371.1 | 349 | UTR 5 | XP_016882860.1 |