Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGCCACCACTTGCCATTCCTAGCG[C/T]GAGACCTGAAAAAAGAGATTCCAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613279 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZC3H14 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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ZC3H14 - zinc finger CCCH-type containing 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160103.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001153575.1 | |
NM_001160104.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001153576.1 | |
NM_001326295.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313224.1 | |
NM_001326296.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313225.1 | |
NM_001326297.1 | 585 | Missense Mutation | GCG,GTG | A,V 88 | NP_001313226.1 | |
NM_001326298.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313227.1 | |
NM_001326299.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313228.1 | |
NM_001326300.1 | 585 | UTR 5 | NP_001313229.1 | |||
NM_001326301.1 | 585 | Missense Mutation | GCG,GTG | A,V 88 | NP_001313230.1 | |
NM_001326302.1 | 585 | UTR 5 | NP_001313231.1 | |||
NM_001326303.1 | 585 | Missense Mutation | GCG,GTG | A,V 88 | NP_001313232.1 | |
NM_001326304.1 | 585 | UTR 5 | NP_001313233.1 | |||
NM_001326305.1 | 585 | UTR 5 | NP_001313234.1 | |||
NM_001326306.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313235.1 | |
NM_001326307.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313236.1 | |
NM_001326308.1 | 585 | UTR 5 | NP_001313237.1 | |||
NM_001326309.1 | 585 | UTR 5 | NP_001313238.1 | |||
NM_001326310.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313239.1 | |
NM_001326311.1 | 585 | UTR 5 | NP_001313240.1 | |||
NM_001326312.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313241.1 | |
NM_001326313.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_001313242.1 | |
NM_001326314.1 | 585 | UTR 5 | NP_001313243.1 | |||
NM_001326315.1 | 585 | Missense Mutation | GCG,GTG | A,V 88 | NP_001313244.1 | |
NM_001326316.1 | 585 | Missense Mutation | GCG,GTG | A,V 88 | NP_001313245.1 | |
NM_024824.4 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_079100.2 | |
NM_207660.3 | 585 | Missense Mutation | GCG,GTG | A,V 122 | NP_997543.1 | |
NM_207661.2 | 585 | Missense Mutation | GCG,GTG | A,V 88 | NP_997544.1 | |
NM_207662.3 | 585 | Intron | NP_997545.2 | |||
XM_005268067.4 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_005268124.1 | |
XM_005268068.4 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_005268125.1 | |
XM_005268069.4 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_005268126.1 | |
XM_005268070.4 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_005268127.1 | |
XM_005268071.4 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_005268128.1 | |
XM_005268073.3 | 585 | Intron | XP_005268130.1 | |||
XM_006720257.2 | 585 | Intron | XP_006720320.1 | |||
XM_011537160.2 | 585 | Missense Mutation | GCG,GTG | A,V 88 | XP_011535462.1 | |
XM_011537161.2 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_011535463.1 | |
XM_011537162.2 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_011535464.1 | |
XM_017021648.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_016877137.1 | |
XM_017021649.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_016877138.1 | |
XM_017021650.1 | 585 | Missense Mutation | GCG,GTG | A,V 122 | XP_016877139.1 |