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GAGCCCAGGCCTGGTCCGTGAGGCT[A/G]TAGAGGGATCCTCTGGGAGGCCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607582 MIM: 607581 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A6 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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SLC22A6 - solute carrier family 22 member 6 | ||||||
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There are no transcripts associated with this gene. |
SLC22A8 - solute carrier family 22 member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184732.1 | 1739 | Nonsense Mutation | CAG,TAG | Q,* 533 | NP_001171661.1 | |
NM_001184733.1 | 1739 | Nonsense Mutation | CAG,TAG | Q,* 442 | NP_001171662.1 | |
NM_001184736.1 | 1739 | Nonsense Mutation | CAG,TAG | Q,* 410 | NP_001171665.1 | |
NM_004254.3 | 1739 | Nonsense Mutation | CAG,TAG | Q,* 533 | NP_004245.2 | |
XM_011545364.1 | 1739 | Nonsense Mutation | CAG,TAG | Q,* 410 | XP_011543666.1 |