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GGGCACAGTCCATCACGGAGCGCAG[G/A]CGGTGGGCAATGAGCAGCACAGTGC
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 |
---|---|---|
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 |
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 | 4390 | Intron | NP_001072996.1 | |||
NM_001171.5 | 4390 | Silent Mutation | NP_001162.4 | |||
XM_011522479.2 | 4390 | Silent Mutation | XP_011520781.1 | |||
XM_011522480.1 | 4390 | Silent Mutation | XP_011520782.1 | |||
XM_011522481.2 | 4390 | Silent Mutation | XP_011520783.1 | |||
XM_011522482.2 | 4390 | Intron | XP_011520784.1 | |||
XM_017023212.1 | 4390 | Silent Mutation | XP_016878701.1 | |||
XM_017023213.1 | 4390 | Silent Mutation | XP_016878702.1 | |||
XM_017023214.1 | 4390 | Intron | XP_016878703.1 |