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TTCGTTGCATCGGCAGGGCCTCACT[A/G]AGGCGTGTCCTCTCAAGTGCTTGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603430 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF202 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZNF202 - zinc finger protein 202 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301779.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | NP_001288708.1 | |
NM_001301780.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | NP_001288709.1 | |
NM_001301819.1 | 2366 | Missense Mutation | TCA,TTA | S,L 365 | NP_001288748.1 | |
NM_003455.3 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | NP_003446.2 | |
XM_005271659.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_005271716.1 | |
XM_005271660.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_005271717.1 | |
XM_005271661.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_005271718.1 | |
XM_005271664.1 | 2366 | Missense Mutation | TCA,TTA | S,L 365 | XP_005271721.1 | |
XM_006718901.2 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_006718964.1 | |
XM_011542972.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_011541274.1 | |
XM_011542973.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_011541275.1 | |
XM_011542975.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_011541277.1 | |
XM_011542976.1 | 2366 | Missense Mutation | TCA,TTA | S,L 365 | XP_011541278.1 | |
XM_017018268.1 | 2366 | Missense Mutation | TCA,TTA | S,L 589 | XP_016873757.1 |