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GCGCACAAAGCGCTTCCCGCACTGC[A/G]GACAGGCGTAGGGCTTCTCGCCCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZSCAN10 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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ZSCAN10 - zinc finger and SCAN domain containing 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282415.1 | 1669 | Missense Mutation | CCG,CTG | P,L 187 | NP_001269344.1 | |
NM_001282416.1 | 1669 | Missense Mutation | CCG,CTG | P,L 444 | NP_001269345.1 | |
NM_032805.2 | 1669 | Missense Mutation | CCG,CTG | P,L 581 | NP_116194.2 | |
XM_017023791.1 | 1669 | Missense Mutation | CCG,CTG | P,L 581 | XP_016879280.1 | |
XM_017023792.1 | 1669 | Missense Mutation | CCG,CTG | P,L 549 | XP_016879281.1 |