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AGGCGCTCCTGGCCTGGGCTGGCCC[C/T]GCCTCCCACTCTGAACCCTCTGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602110 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC102724064 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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LOC102724064 - uncharacterized LOC102724064 | ||||||
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There are no transcripts associated with this gene. |
SLC29A2 - solute carrier family 29 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300868.1 | 2110 | UTR 3 | NP_001287797.1 | |||
NM_001300869.1 | 2110 | UTR 3 | NP_001287798.1 | |||
NM_001532.2 | 2110 | UTR 3 | NP_001523.2 | |||
XM_011544974.1 | 2110 | UTR 3 | XP_011543276.1 | |||
XM_017017630.1 | 2110 | UTR 3 | XP_016873119.1 | |||
XM_017017631.1 | 2110 | Intron | XP_016873120.1 | |||
XM_017017632.1 | 2110 | UTR 3 | XP_016873121.1 | |||
XM_017017633.1 | 2110 | Intron | XP_016873122.1 | |||
XM_017017634.1 | 2110 | Intron | XP_016873123.1 | |||
XM_017017635.1 | 2110 | UTR 3 | XP_016873124.1 | |||
XM_017017636.1 | 2110 | Intron | XP_016873125.1 | |||
XM_017017637.1 | 2110 | UTR 3 | XP_016873126.1 | |||
XM_017017638.1 | 2110 | UTR 3 | XP_016873127.1 |