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ACGAATTGCACCAGGCAATACGCTA[C/T]AGTATCTGATAACTAGTACACAATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300516 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATP11C PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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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ATP11C - ATPase phospholipid transporting 11C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010986.2 | Intron | NP_001010986.1 | ||||
NM_173694.4 | Intron | NP_775965.2 | ||||
XM_017029439.1 | Intron | XP_016884928.1 | ||||
XM_017029440.1 | Intron | XP_016884929.1 | ||||
XM_017029441.1 | Intron | XP_016884930.1 | ||||
XM_017029442.1 | Intron | XP_016884931.1 | ||||
XM_017029443.1 | Intron | XP_016884932.1 | ||||
XM_017029444.1 | Intron | XP_016884933.1 | ||||
XM_017029445.1 | Intron | XP_016884934.1 | ||||
XM_017029446.1 | Intron | XP_016884935.1 | ||||
XM_017029447.1 | Intron | XP_016884936.1 | ||||
XM_017029448.1 | Intron | XP_016884937.1 | ||||
XM_017029449.1 | Intron | XP_016884938.1 |