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CACTCACTACCACGCCTCTTCTGTA[C/G]ACACCCTGCACATGGCTAAGGCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610238 | ||||||||||||||||||||
Literature Links: |
SLC5A11 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 |
SLC5A11 - solute carrier family 5 member 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258411.2 | 366 | Intron | NP_001245340.1 | |||
NM_001258412.2 | 366 | Intron | NP_001245341.1 | |||
NM_001258413.2 | 366 | Intron | NP_001245342.1 | |||
NM_001258414.1 | 366 | Intron | NP_001245343.1 | |||
NM_052944.4 | 366 | Intron | NP_443176.2 | |||
XM_005255080.2 | 366 | Intron | XP_005255137.1 | |||
XM_005255082.4 | 366 | Intron | XP_005255139.1 | |||
XM_006721015.2 | 366 | Intron | XP_006721078.1 | |||
XM_011545725.2 | 366 | Intron | XP_011544027.2 | |||
XM_011545728.1 | 366 | Intron | XP_011544030.1 | |||
XM_017022900.1 | 366 | Intron | XP_016878389.1 | |||
XM_017022901.1 | 366 | UTR 5 | XP_016878390.1 | |||
XM_017022902.1 | 366 | Intron | XP_016878391.1 | |||
XM_017022903.1 | 366 | Intron | XP_016878392.1 | |||
XM_017022904.1 | 366 | Intron | XP_016878393.1 | |||
XM_017022905.1 | 366 | Intron | XP_016878394.1 | |||
XM_017022906.1 | 366 | Intron | XP_016878395.1 | |||
XM_017022907.1 | 366 | Intron | XP_016878396.1 | |||
XM_017022908.1 | 366 | Intron | XP_016878397.1 | |||
XM_017022909.1 | 366 | Intron | XP_016878398.1 |