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TCCACCTACAGAACCACAAGCAGCA[A/G]TCTCCGAGCTGACCAGGAGGCACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612373 | ||||||||||||||||||||
Literature Links: |
SLC29A3 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 |
SLC29A3 - solute carrier family 29 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174098.1 | 125 | Missense Mutation | AAT,AGT | N,S 23 | NP_001167569.1 | |
NM_018344.5 | 125 | Missense Mutation | AAT,AGT | N,S 23 | NP_060814.4 | |
XM_006717910.3 | 125 | UTR 5 | XP_006717973.1 | |||
XM_017016377.1 | 125 | UTR 5 | XP_016871866.1 | |||
XM_017016378.1 | 125 | UTR 5 | XP_016871867.1 |