Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGATGGCTGCTCCTCTTTGAGCAC[C/T]GGCACATATCAGTCTGTCCTCTTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ATP10B 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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ATP10B - ATPase phospholipid transporting 10B (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025153.2 | 4738 | Missense Mutation | CAG,CGG | Q,R 1445 | NP_079429.2 | |
XM_006714833.2 | 4738 | Missense Mutation | CAG,CGG | Q,R 1445 | XP_006714896.1 | |
XM_011534468.2 | 4738 | Missense Mutation | CAG,CGG | Q,R 1445 | XP_011532770.1 | |
XM_011534469.1 | 4738 | Missense Mutation | CAG,CGG | Q,R 1445 | XP_011532771.1 | |
XM_011534472.2 | 4738 | Missense Mutation | CAG,CGG | Q,R 1417 | XP_011532774.1 | |
XM_017009252.1 | 4738 | Missense Mutation | CAG,CGG | Q,R 1433 | XP_016864741.1 | |
XM_017009253.1 | 4738 | Missense Mutation | CAG,CGG | Q,R 1378 | XP_016864742.1 |