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Search Thermo Fisher Scientific
TCTCCAGTGTGAGTTCTTTGATGTG[C/T]AACAAGCTGAGAGCTCCAGCTGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606740 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF180 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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ZNF180 - zinc finger protein 180 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278508.2 | 1773 | Missense Mutation | ACA,GCA | T,A 513 | NP_001265437.2 | |
NM_001278509.2 | 1773 | Missense Mutation | ACA,GCA | T,A 511 | NP_001265438.2 | |
NM_001288759.2 | 1773 | Missense Mutation | ACA,GCA | T,A 537 | NP_001275688.2 | |
NM_001288760.2 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | NP_001275689.1 | |
NM_001288761.2 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | NP_001275690.1 | |
NM_001288762.2 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | NP_001275691.1 | |
NM_001291633.1 | 1773 | Missense Mutation | ACA,GCA | T,A 511 | NP_001278562.1 | |
NM_013256.5 | 1773 | Missense Mutation | ACA,GCA | T,A 538 | NP_037388.3 | |
XM_011527280.2 | 1773 | Missense Mutation | ACA,GCA | T,A 580 | XP_011525582.1 | |
XM_017027250.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882739.1 | |
XM_017027251.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882740.1 | |
XM_017027252.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882741.1 | |
XM_017027253.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882742.1 | |
XM_017027254.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882743.1 | |
XM_017027255.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882744.1 | |
XM_017027256.1 | 1773 | Missense Mutation | ACA,GCA | T,A 195 | XP_016882745.1 |