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TTCTGGAGTATACGTTATCCTTCCT[A/G]ATAGCCCTGAATAAGGAAATAATAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614955 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLFN12 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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SLFN12 - schlafen family member 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289009.1 | 1663 | Missense Mutation | TCA,TTA | S,L 385 | NP_001275938.1 | |
NM_018042.4 | 1663 | Missense Mutation | TCA,TTA | S,L 385 | NP_060512.3 | |
XM_005257995.4 | 1663 | Missense Mutation | TCA,TTA | S,L 385 | XP_005258052.1 | |
XM_011524967.2 | 1663 | Missense Mutation | TCA,TTA | S,L 385 | XP_011523269.1 | |
XM_017024809.1 | 1663 | Missense Mutation | TCA,TTA | S,L 385 | XP_016880298.1 | |
XM_017024810.1 | 1663 | Missense Mutation | TCA,TTA | S,L 385 | XP_016880299.1 | |
XM_017024811.1 | 1663 | UTR 3 | XP_016880300.1 |