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AGAAAGGCTATTTCAAACTGTGACA[A/G]GTACTTTAAAGAAAATAAAGGTAAA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610803 | |||||||||||||||||||||||
Literature Links: |
SLC41A3 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
SLC41A3 - solute carrier family 41 member 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008485.1 | Intron | NP_001008485.1 | ||||
NM_001008486.1 | Intron | NP_001008486.1 | ||||
NM_001008487.1 | Intron | NP_001008487.1 | ||||
NM_001164475.1 | Intron | NP_001157947.1 | ||||
NM_017836.3 | Intron | NP_060306.3 | ||||
XM_005247559.1 | Intron | XP_005247616.1 | ||||
XM_005247562.1 | Intron | XP_005247619.1 | ||||
XM_005247563.2 | Intron | XP_005247620.1 | ||||
XM_005247564.1 | Intron | XP_005247621.1 | ||||
XM_005247565.2 | Intron | XP_005247622.1 | ||||
XM_006713681.2 | Intron | XP_006713744.1 | ||||
XM_011512945.1 | Intron | XP_011511247.1 | ||||
XM_017006705.1 | Intron | XP_016862194.1 | ||||
XM_017006706.1 | Intron | XP_016862195.1 | ||||
XM_017006707.1 | Intron | XP_016862196.1 | ||||
XM_017006708.1 | Intron | XP_016862197.1 | ||||
XM_017006709.1 | Intron | XP_016862198.1 |