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GTCAAGAAATCTATGGGGAAAGCCA[C/T]GCATGGTTCTGTGACAGTGGAGATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610238 MIM: 610739 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC5A11 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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SLC5A11 - solute carrier family 5 member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258411.2 | Intron | NP_001245340.1 | ||||
NM_001258412.2 | Intron | NP_001245341.1 | ||||
NM_001258413.2 | Intron | NP_001245342.1 | ||||
NM_001258414.1 | Intron | NP_001245343.1 | ||||
NM_052944.4 | Intron | NP_443176.2 | ||||
XM_005255080.2 | Intron | XP_005255137.1 | ||||
XM_005255082.4 | Intron | XP_005255139.1 | ||||
XM_006721015.2 | Intron | XP_006721078.1 | ||||
XM_011545725.2 | Intron | XP_011544027.2 | ||||
XM_011545728.1 | Intron | XP_011544030.1 | ||||
XM_017022900.1 | Intron | XP_016878389.1 | ||||
XM_017022901.1 | Intron | XP_016878390.1 | ||||
XM_017022902.1 | Intron | XP_016878391.1 | ||||
XM_017022903.1 | Intron | XP_016878392.1 | ||||
XM_017022904.1 | Intron | XP_016878393.1 | ||||
XM_017022905.1 | Intron | XP_016878394.1 | ||||
XM_017022906.1 | Intron | XP_016878395.1 | ||||
XM_017022907.1 | Intron | XP_016878396.1 | ||||
XM_017022908.1 | Intron | XP_016878397.1 | ||||
XM_017022909.1 | Intron | XP_016878398.1 |
TNRC6A - trinucleotide repeat containing 6A | ||||||
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There are no transcripts associated with this gene. |