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GGCCTGCATCTGCAGCTCCGTGCCA[A/G]GGTCCACGGCAGCAGTAGCCTCGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 158343 MIM: 603234 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ABCC1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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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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ABCC1 - ATP binding cassette subfamily C member 1 | ||||||
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There are no transcripts associated with this gene. |
ABCC6 - ATP binding cassette subfamily C member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079528.3 | 4314 | Intron | NP_001072996.1 | |||
NM_001171.5 | 4314 | Missense Mutation | CCT,CTT | P,L 1434 | NP_001162.4 | |
XM_011522479.2 | 4314 | Missense Mutation | CCT,CTT | P,L 1423 | XP_011520781.1 | |
XM_011522480.1 | 4314 | Missense Mutation | CCT,CTT | P,L 1320 | XP_011520782.1 | |
XM_011522481.2 | 4314 | Missense Mutation | CCT,CTT | P,L 1320 | XP_011520783.1 | |
XM_011522482.2 | 4314 | Intron | XP_011520784.1 | |||
XM_017023212.1 | 4314 | Missense Mutation | CCT,CTT | P,L 1378 | XP_016878701.1 | |
XM_017023213.1 | 4314 | Missense Mutation | CCT,CTT | P,L 1320 | XP_016878702.1 | |
XM_017023214.1 | 4314 | Intron | XP_016878703.1 |