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TTTCAGGGAGGGAGAGGATAACCAA[C/T]CTCCCTTTTTGAGAGCAAGACCGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607580 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A10 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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SLC22A10 - solute carrier family 22 member 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039752.3 | Intron | NP_001034841.3 | ||||
XM_011545016.2 | Intron | XP_011543318.1 | ||||
XM_017017699.1 | Intron | XP_016873188.1 | ||||
XM_017017700.1 | Intron | XP_016873189.1 | ||||
XM_017017701.1 | Intron | XP_016873190.1 | ||||
XM_017017702.1 | Intron | XP_016873191.1 | ||||
XM_017017703.1 | Intron | XP_016873192.1 | ||||
XM_017017704.1 | Intron | XP_016873193.1 |