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GAATGTCTAATACTTCTGCCTCACC[A/C]ACCCAGTAACTAAATGCCACTAGCA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605869 | |||||||||||||||||||||||
Literature Links: |
ATP11B PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
ATP11B - ATPase phospholipid transporting 11B (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014616.2 | Intron | NP_055431.1 | ||||
XM_005247241.2 | Intron | XP_005247298.1 | ||||
XM_005247243.2 | Intron | XP_005247300.1 | ||||
XM_011512593.2 | Intron | XP_011510895.1 | ||||
XM_011512594.2 | Intron | XP_011510896.1 | ||||
XM_011512597.2 | Intron | XP_011510899.1 | ||||
XM_017006008.1 | Intron | XP_016861497.1 | ||||
XM_017006009.1 | Intron | XP_016861498.1 |