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CTCCCCTGGGCATGCAGGCTTGGGC[A/G]TGGAAATCTCTTTGGGCTCCATGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616776 MIM: 602939 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DUSP15 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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DUSP15 - dual specificity phosphatase 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012644.2 | 665 | Intron | NP_001012662.1 | |||
NM_001320478.1 | 665 | Intron | NP_001307407.1 | |||
NM_001320479.1 | 665 | Intron | NP_001307408.1 | |||
NM_080611.4 | 665 | Intron | NP_542178.2 | |||
NM_177991.2 | 665 | Intron | NP_817130.1 | |||
XM_017027654.1 | 665 | Intron | XP_016883143.1 | |||
XM_017027655.1 | 665 | Intron | XP_016883144.1 | |||
XM_017027656.1 | 665 | Intron | XP_016883145.1 | |||
XM_017027657.1 | 665 | Intron | XP_016883146.1 | |||
XM_017027658.1 | 665 | Intron | XP_016883147.1 | |||
XM_017027659.1 | 665 | Intron | XP_016883148.1 | |||
XM_017027660.1 | 665 | Intron | XP_016883149.1 | |||
XM_017027661.1 | 665 | Intron | XP_016883150.1 | |||
XM_017027662.1 | 665 | Intron | XP_016883151.1 |
FOXS1 - forkhead box S1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004118.3 | 665 | Missense Mutation | NP_004109.1 |