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CCCCCAACAGGGCACCTTCAGCCTG[C/T]GGAAGCTATGGGCCTTCACGGGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600266 | ||||||||||||||||||||
Literature Links: |
SLC11A1 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 |
SLC11A1 - solute carrier family 11 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000578.3 | 769 | Missense Mutation | CGG,TGG | R,W 56 | NP_000569.3 | |
XM_005246793.3 | 769 | UTR 5 | XP_005246850.1 | |||
XM_005246794.3 | 769 | UTR 5 | XP_005246851.1 | |||
XM_006712709.3 | 769 | UTR 5 | XP_006712772.1 | |||
XM_006712710.3 | 769 | Intron | XP_006712773.1 | |||
XM_006712711.3 | 769 | Intron | XP_006712774.1 | |||
XM_011511684.2 | 769 | UTR 5 | XP_011509986.1 | |||
XM_011511685.2 | 769 | UTR 5 | XP_011509987.1 | |||
XM_017004765.1 | 769 | Intron | XP_016860254.1 | |||
XM_017004766.1 | 769 | UTR 5 | XP_016860255.1 | |||
XM_017004767.1 | 769 | Missense Mutation | CGG,TGG | R,W 56 | XP_016860256.1 |