Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGATTTACAAACTAGTTACATTCA[C/T]AGAGTTTCTCTTCAGTATGAGTTGC
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 2227 | Missense Mutation | TAT,TGT | Y,C 664 | NP_001265437.2 | |
NM_001278509.2 | 2227 | Missense Mutation | TAT,TGT | Y,C 662 | NP_001265438.2 | |
NM_001288759.2 | 2227 | Missense Mutation | TAT,TGT | Y,C 688 | NP_001275688.2 | |
NM_001288760.2 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | NP_001275689.1 | |
NM_001288761.2 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | NP_001275690.1 | |
NM_001288762.2 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | NP_001275691.1 | |
NM_001291633.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 662 | NP_001278562.1 | |
NM_013256.5 | 2227 | Missense Mutation | TAT,TGT | Y,C 689 | NP_037388.3 | |
XM_011527280.2 | 2227 | Missense Mutation | TAT,TGT | Y,C 731 | XP_011525582.1 | |
XM_017027250.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882739.1 | |
XM_017027251.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882740.1 | |
XM_017027252.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882741.1 | |
XM_017027253.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882742.1 | |
XM_017027254.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882743.1 | |
XM_017027255.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882744.1 | |
XM_017027256.1 | 2227 | Missense Mutation | TAT,TGT | Y,C 346 | XP_016882745.1 |