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TGGAAGATTTCATTTAAAGATACAG[C/T]ACCATGGCTAAAACCAACCCCAAAA
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)
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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 | Intron | NP_001287797.1 | ||||
NM_001300869.1 | Intron | NP_001287798.1 | ||||
NM_001532.2 | Intron | NP_001523.2 | ||||
XM_011544974.1 | Intron | XP_011543276.1 | ||||
XM_017017630.1 | Intron | XP_016873119.1 | ||||
XM_017017631.1 | Intron | XP_016873120.1 | ||||
XM_017017632.1 | Intron | XP_016873121.1 | ||||
XM_017017633.1 | Intron | XP_016873122.1 | ||||
XM_017017634.1 | Intron | XP_016873123.1 | ||||
XM_017017635.1 | Intron | XP_016873124.1 | ||||
XM_017017636.1 | Intron | XP_016873125.1 | ||||
XM_017017637.1 | Intron | XP_016873126.1 | ||||
XM_017017638.1 | Intron | XP_016873127.1 |
Set Membership: |
HapMap |