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AAAGTTTAAATATTTCTGAGAAAGG[A/C]CTCTGCTGCTGTTACGCTGACCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601872 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC7A2 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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SLC7A2 - solute carrier family 7 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008539.3 | 40 | Intron | NP_001008539.3 | |||
NM_001164771.1 | 40 | Intron | NP_001158243.1 | |||
NM_003046.5 | 40 | Intron | NP_003037.4 | |||
XM_005273610.4 | 40 | Intron | XP_005273667.1 | |||
XM_005273611.4 | 40 | UTR 5 | XP_005273668.1 | |||
XM_005273612.4 | 40 | Intron | XP_005273669.1 | |||
XM_017013746.1 | 40 | Intron | XP_016869235.1 | |||
XM_017013747.1 | 40 | Intron | XP_016869236.1 |