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CCCTGGCCCAGTCCACCGGCCGCCA[A/G]CACGCGGGGGTCGTAGGGAGCGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZC3H4 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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ZC3H4 - zinc finger CCCH-type containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015168.1 | 4689 | Silent Mutation | CTG,TTG | L,L 1126 | NP_055983.1 | |
XM_005258676.3 | 4689 | Silent Mutation | CTG,TTG | L,L 1090 | XP_005258733.1 | |
XM_005258677.4 | 4689 | Silent Mutation | CTG,TTG | L,L 1085 | XP_005258734.1 | |
XM_005258678.2 | 4689 | Silent Mutation | CTG,TTG | L,L 1077 | XP_005258735.1 | |
XM_006723113.3 | 4689 | Silent Mutation | CTG,TTG | L,L 1126 | XP_006723176.1 | |
XM_011526668.2 | 4689 | Silent Mutation | CTG,TTG | L,L 1085 | XP_011524970.1 | |
XM_011526669.2 | 4689 | Silent Mutation | CTG,TTG | L,L 1080 | XP_011524971.1 | |
XM_011526670.2 | 4689 | Silent Mutation | CTG,TTG | L,L 1076 | XP_011524972.1 | |
XM_017026529.1 | 4689 | Silent Mutation | CTG,TTG | L,L 1113 | XP_016882018.1 | |
XM_017026530.1 | 4689 | Silent Mutation | CTG,TTG | L,L 1042 | XP_016882019.1 | |
XM_017026531.1 | 4689 | Silent Mutation | CTG,TTG | L,L 829 | XP_016882020.1 |