Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACTATCCGGGTCCTTTCCTTTCC[C/T]CCAGAAGTGATGGACCATCCAGTCA
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 - Not Available | 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 |
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 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | NP_115524.3 | |
XM_005269176.1 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_005269233.1 | |
XM_005269178.1 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_005269235.1 | |
XM_005269179.1 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_005269236.1 | |
XM_006719630.2 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_006719693.1 | |
XM_011538807.2 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_011537109.1 | |
XM_011538808.1 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_011537110.1 | |
XM_011538809.1 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_011537111.1 | |
XM_011538810.2 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_011537112.1 | |
XM_011538811.2 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_011537113.1 | |
XM_011538813.2 | 2113 | Missense Mutation | AGG,GGG | R,G 303 | XP_011537115.1 | |
XM_017020013.1 | 2113 | Missense Mutation | AGG,GGG | R,G 529 | XP_016875502.1 | |
XM_017020014.1 | 2113 | UTR 3 | XP_016875503.1 | |||
XM_017020015.1 | 2113 | Intron | XP_016875504.1 | |||
XM_017020016.1 | 2113 | Missense Mutation | AGG,GGG | R,G 318 | XP_016875505.1 | |
XM_017020017.1 | 2113 | Missense Mutation | AGG,GGG | R,G 317 | XP_016875506.1 |