Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATAAAGGTTTCCCCACACTCCTGA[C/T]ACTCATAGGGCTTCTCCCCTGTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 194528 | ||||||||||||||||||||
Literature Links: |
ZNF25 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 |
ZNF25 - zinc finger protein 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005252384.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 428 | XP_005252441.1 | |
XM_005252385.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 428 | XP_005252442.1 | |
XM_005252386.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 428 | XP_005252443.1 | |
XM_011519352.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 432 | XP_011517654.1 | |
XM_011519353.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 432 | XP_011517655.1 | |
XM_011519354.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 432 | XP_011517656.1 | |
XM_011519355.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 432 | XP_011517657.1 | |
XM_011519356.2 | 1626 | Missense Mutation | TAT,TGT | Y,C 392 | XP_011517658.1 | |
XM_017015837.1 | 1626 | Missense Mutation | TAT,TGT | Y,C 392 | XP_016871326.1 | |
XM_017015838.1 | 1626 | Missense Mutation | TAT,TGT | Y,C 392 | XP_016871327.1 |