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ATGGCAGTGTGTGCAAAAAAGCGCC[C/T]CCCAGGTAAGACAGGCAAGGAGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 606578 MIM: 605867 | ||||||||||||||||||||
Literature Links: |
AQP10 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
AQP10 - aquaporin 10 | ||||||
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There are no transcripts associated with this gene. |
ATP8B2 - ATPase phospholipid transporting 8B2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005855.1 | 225 | Missense Mutation | CCC,CTC | P,L 9 | NP_001005855.1 | |
NM_020452.3 | 225 | Missense Mutation | CCC,CTC | P,L 42 | NP_065185.1 | |
XM_005245355.2 | 225 | Intron | XP_005245412.1 | |||
XM_005245356.3 | 225 | Missense Mutation | CCC,CTC | P,L 9 | XP_005245413.1 | |
XM_017001871.1 | 225 | Intron | XP_016857360.1 | |||
XM_017001872.1 | 225 | Missense Mutation | CCC,CTC | P,L 9 | XP_016857361.1 |