Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCTCAGCACTACCTGTTCTGCAGG[C/T]GGGTCCTGGCCTCCCCGCAGTGAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZSCAN25 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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ZSCAN25 - zinc finger and SCAN domain containing 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145115.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | NP_660090.2 | |
XM_005250194.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_005250251.1 | |
XM_011515905.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_011514207.1 | |
XM_011515906.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_011514208.1 | |
XM_011515907.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_011514209.1 | |
XM_011515908.2 | 1190 | Missense Mutation | GCG,GTG | A,V 39 | XP_011514210.1 | |
XM_011515909.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_011514211.1 | |
XM_011515910.2 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_011514212.1 | |
XM_017011824.1 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_016867313.1 | |
XM_017011825.1 | 1190 | Missense Mutation | GCG,GTG | A,V 39 | XP_016867314.1 | |
XM_017011826.1 | 1190 | Missense Mutation | GCG,GTG | A,V 39 | XP_016867315.1 | |
XM_017011827.1 | 1190 | Missense Mutation | GCG,GTG | A,V 203 | XP_016867316.1 |