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ACTGTTTCAGATCCTCTGGGAGGAC[A/G]AGTTTGGTTATCTTATGATGCTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300890 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASB9 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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ASB9 - ankyrin repeat and SOCS box containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031739.2 | 1388 | Intron | NP_001026909.1 | |||
NM_001168530.1 | 1388 | Intron | NP_001162002.1 | |||
NM_001168531.1 | 1388 | UTR 3 | NP_001162003.1 | |||
NM_024087.2 | 1388 | Intron | NP_076992.1 | |||
XM_005274446.1 | 1388 | Silent Mutation | CTC,CTT | L,L 281 | XP_005274503.1 | |
XM_011545458.1 | 1388 | Silent Mutation | CTC,CTT | L,L 252 | XP_011543760.1 | |
XM_011545460.1 | 1388 | UTR 3 | XP_011543762.1 | |||
XM_017029283.1 | 1388 | Silent Mutation | CTC,CTT | L,L 364 | XP_016884772.1 | |
XM_017029284.1 | 1388 | Silent Mutation | CTC,CTT | L,L 335 | XP_016884773.1 | |
XM_017029285.1 | 1388 | UTR 3 | XP_016884774.1 | |||
XM_017029286.1 | 1388 | UTR 3 | XP_016884775.1 |