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GCCGGCACTGCTCACCAAGCCTGCC[A/G]CTTCCAGGTGAGTAGACAGGCCCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610408 | ||||||||||||||||||||
Literature Links: |
SLC15A3 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 |
SLC15A3 - solute carrier family 15 member 3 | ||||||
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There are no transcripts associated with this gene. |
TMEM109 - transmembrane protein 109 | ||||||
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There are no transcripts associated with this gene. |
TMEM132A - transmembrane protein 132A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017870.3 | 720 | Missense Mutation | CAC,CGC | H,R 176 | NP_060340.2 | |
NM_178031.2 | 720 | Missense Mutation | CAC,CGC | H,R 176 | NP_821174.1 | |
XM_017017951.1 | 720 | Missense Mutation | CAC,CGC | H,R 189 | XP_016873440.1 | |
XM_017017952.1 | 720 | Missense Mutation | CAC,CGC | H,R 189 | XP_016873441.1 |