Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCAGGGAACAGGCTGATAAATATTA[G/T]AAGAATTATAGCCAACCATGTGGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300516 | ||||||||||||||||||||
Literature Links: |
ATP11C PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
ATP11C - ATPase phospholipid transporting 11C | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010986.2 | 3942 | Silent Mutation | NP_001010986.1 | |||
NM_173694.4 | 3942 | Silent Mutation | NP_775965.2 | |||
XM_017029439.1 | 3942 | Silent Mutation | XP_016884928.1 | |||
XM_017029440.1 | 3942 | Silent Mutation | XP_016884929.1 | |||
XM_017029441.1 | 3942 | Silent Mutation | XP_016884930.1 | |||
XM_017029442.1 | 3942 | Silent Mutation | XP_016884931.1 | |||
XM_017029443.1 | 3942 | Silent Mutation | XP_016884932.1 | |||
XM_017029444.1 | 3942 | Silent Mutation | XP_016884933.1 | |||
XM_017029445.1 | 3942 | Silent Mutation | XP_016884934.1 | |||
XM_017029446.1 | 3942 | Silent Mutation | XP_016884935.1 | |||
XM_017029447.1 | 3942 | Silent Mutation | XP_016884936.1 | |||
XM_017029448.1 | 3942 | Missense Mutation | XP_016884937.1 | |||
XM_017029449.1 | 3942 | Silent Mutation | XP_016884938.1 |