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GCAAAGAAGTGGGCAGGTTTTCTTT[C/T]TGCCTGCAGAAGGCTTCTCAAATGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608094 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC37A1 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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SLC37A1 - solute carrier family 37 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320537.1 | Intron | NP_001307466.1 | ||||
NM_018964.3 | Intron | NP_061837.3 | ||||
XM_011529614.2 | Intron | XP_011527916.1 | ||||
XM_011529615.1 | Intron | XP_011527917.1 | ||||
XM_017028376.1 | Intron | XP_016883865.1 | ||||
XM_017028377.1 | Intron | XP_016883866.1 | ||||
XM_017028378.1 | Intron | XP_016883867.1 | ||||
XM_017028379.1 | Intron | XP_016883868.1 | ||||
XM_017028380.1 | Intron | XP_016883869.1 | ||||
XM_017028381.1 | Intron | XP_016883870.1 | ||||
XM_017028382.1 | Intron | XP_016883871.1 | ||||
XM_017028383.1 | Intron | XP_016883872.1 |
Set Membership: |
HapMap |