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CAAACGTGATTAAGGGTCACAGAAG[A/G]GAAGAATGATGAACGAATTGCTGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 158378 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC20A2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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
|
SLC20A2 - solute carrier family 20 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257180.1 | Intron | NP_001244109.1 | ||||
NM_001257181.1 | Intron | NP_001244110.1 | ||||
NM_006749.4 | Intron | NP_006740.1 | ||||
XM_005273613.3 | Intron | XP_005273670.1 | ||||
XM_005273615.3 | Intron | XP_005273672.1 | ||||
XM_006716390.3 | Intron | XP_006716453.1 | ||||
XM_006716391.3 | Intron | XP_006716454.1 | ||||
XM_017013748.1 | Intron | XP_016869237.1 | ||||
XM_017013749.1 | Intron | XP_016869238.1 | ||||
XM_017013750.1 | Intron | XP_016869239.1 | ||||
XM_017013751.1 | Intron | XP_016869240.1 | ||||
XM_017013752.1 | Intron | XP_016869241.1 |