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Search Thermo Fisher Scientific
ACTGGAAGAGTCCCAGCTCCGAGTT[C/T]GAGAGACAATGGGACCAGGGCTCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZC3HC1 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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ZC3HC1 - zinc finger C3HC-type containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282190.1 | 1639 | Missense Mutation | CAA,CGA | Q,R 330 | NP_001269119.1 | |
NM_001282191.1 | 1639 | Intron | NP_001269120.1 | |||
NM_016478.4 | 1639 | Missense Mutation | CAA,CGA | Q,R 351 | NP_057562.3 | |
XM_005250403.2 | 1639 | Missense Mutation | CAA,CGA | Q,R 227 | XP_005250460.1 | |
XM_011516288.2 | 1639 | Missense Mutation | CAA,CGA | Q,R 284 | XP_011514590.1 | |
XM_011516289.2 | 1639 | Missense Mutation | CAA,CGA | Q,R 261 | XP_011514591.1 | |
XM_011516290.2 | 1639 | Missense Mutation | CAA,CGA | Q,R 183 | XP_011514592.1 | |
XM_017012287.1 | 1639 | Missense Mutation | CAA,CGA | Q,R 308 | XP_016867776.1 | |
XM_017012288.1 | 1639 | Missense Mutation | CAA,CGA | Q,R 183 | XP_016867777.1 |