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CCAAGATGGCTATGGCTCTTCTTAC[C/T]GTCTTTTGCTGAGCTGACAATCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606105 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC44A1 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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SLC44A1 - solute carrier family 44 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286730.1 | Intron | NP_001273659.1 | ||||
NM_080546.4 | Intron | NP_536856.2 | ||||
XM_005251855.4 | Intron | XP_005251912.1 | ||||
XM_006717027.3 | Intron | XP_006717090.1 | ||||
XM_006717028.3 | Intron | XP_006717091.1 | ||||
XM_006717029.2 | Intron | XP_006717092.1 | ||||
XM_017014559.1 | Intron | XP_016870048.1 | ||||
XM_017014560.1 | Intron | XP_016870049.1 |