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AAAGTGAGTTTATCTTATGCTCAGC[A/C]AAACATATTTAGGTCAGTTTAAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610802 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC41A2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
SLC41A2 - solute carrier family 41 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032148.3 | 2779 | UTR 3 | NP_115524.3 | |||
XM_005269176.1 | 2779 | UTR 3 | XP_005269233.1 | |||
XM_005269178.1 | 2779 | UTR 3 | XP_005269235.1 | |||
XM_005269179.1 | 2779 | UTR 3 | XP_005269236.1 | |||
XM_006719630.2 | 2779 | UTR 3 | XP_006719693.1 | |||
XM_011538807.2 | 2779 | UTR 3 | XP_011537109.1 | |||
XM_011538808.1 | 2779 | UTR 3 | XP_011537110.1 | |||
XM_011538809.1 | 2779 | UTR 3 | XP_011537111.1 | |||
XM_011538810.2 | 2779 | UTR 3 | XP_011537112.1 | |||
XM_011538811.2 | 2779 | UTR 3 | XP_011537113.1 | |||
XM_011538813.2 | 2779 | UTR 3 | XP_011537115.1 | |||
XM_017020013.1 | 2779 | UTR 3 | XP_016875502.1 | |||
XM_017020014.1 | 2779 | UTR 3 | XP_016875503.1 | |||
XM_017020015.1 | 2779 | Intron | XP_016875504.1 | |||
XM_017020016.1 | 2779 | UTR 3 | XP_016875505.1 | |||
XM_017020017.1 | 2779 | UTR 3 | XP_016875506.1 |