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TGAGGGCTGCGAACAATGACCCAGG[A/C]TTCTTCCGCAGTACCTCCGGCCGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607040 | ||||||||||||||||||||
Literature Links: |
ABCC11 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 |
ABCC11 - ATP binding cassette subfamily C member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032583.3 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | NP_115972.2 | |
NM_033151.3 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | NP_149163.2 | |
NM_145186.2 | 4445 | Missense Mutation | AAG,AAT | K,N 1327 | NP_660187.1 | |
XM_011523397.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1046 | XP_011521699.1 | |
XM_011523398.2 | 4445 | Missense Mutation | AAG,AAT | K,N 742 | XP_011521700.1 | |
XM_017023795.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | XP_016879284.1 | |
XM_017023796.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | XP_016879285.1 | |
XM_017023797.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | XP_016879286.1 | |
XM_017023798.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | XP_016879287.1 | |
XM_017023799.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | XP_016879288.1 | |
XM_017023800.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1365 | XP_016879289.1 | |
XM_017023801.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1329 | XP_016879290.1 | |
XM_017023802.1 | 4445 | Missense Mutation | AAG,AAT | K,N 1046 | XP_016879291.1 | |
XM_017023803.1 | 4445 | Intron | XP_016879292.1 |