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TCAAAGAAGCGCCTGCACGTGTCTG[C/T]CACACAGGTCATTATTTGCTCCACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614953 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLFN11 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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SLFN11 - schlafen family member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001104587.1 | 2712 | Intron | NP_001098057.1 | |||
NM_001104588.1 | 2712 | Intron | NP_001098058.1 | |||
NM_001104589.1 | 2712 | Intron | NP_001098059.1 | |||
NM_001104590.1 | 2712 | Intron | NP_001098060.1 | |||
NM_152270.3 | 2712 | Intron | NP_689483.3 | |||
XM_005258068.3 | 2712 | Missense Mutation | ACA,GCA | T,A 793 | XP_005258125.1 | |
XM_006722171.3 | 2712 | Missense Mutation | ACA,GCA | T,A 793 | XP_006722234.1 | |
XM_011525465.2 | 2712 | Missense Mutation | ACA,GCA | T,A 793 | XP_011523767.1 | |
XM_017025299.1 | 2712 | Missense Mutation | ACA,GCA | T,A 793 | XP_016880788.1 |