Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGTAGTTAGACTTGATCTTACCCT[A/G]AAGGCTTTCCCACACTCTGTACACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600398 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF160 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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ZNF160 - zinc finger protein 160 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102603.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001096073.1 | |
NM_001322125.1 | 2722 | Intron | NP_001309054.1 | |||
NM_001322126.1 | 2722 | Intron | NP_001309055.1 | |||
NM_001322128.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309057.1 | |
NM_001322129.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309058.1 | |
NM_001322130.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309059.1 | |
NM_001322131.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309060.1 | |
NM_001322132.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309061.1 | |
NM_001322133.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309062.1 | |
NM_001322134.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309063.1 | |
NM_001322135.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309064.1 | |
NM_001322136.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_001309065.1 | |
NM_001322137.1 | 2722 | Silent Mutation | TTC,TTT | F,F 734 | NP_001309066.1 | |
NM_001322138.1 | 2722 | Silent Mutation | TTC,TTT | F,F 734 | NP_001309067.1 | |
NM_001322139.1 | 2722 | Silent Mutation | TTC,TTT | F,F 734 | NP_001309068.1 | |
NM_033288.3 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_150630.2 | |
NM_198893.2 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | NP_942596.1 | |
XM_017027445.1 | 2722 | Silent Mutation | TTC,TTT | F,F 789 | XP_016882934.1 | |
XM_017027446.1 | 2722 | Silent Mutation | TTC,TTT | F,F 770 | XP_016882935.1 | |
XM_017027447.1 | 2722 | Intron | XP_016882936.1 | |||
XM_017027448.1 | 2722 | Intron | XP_016882937.1 |