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AGCCCAGTGCCAAGCAGGTCCCCCA[C/G]AGCAGTCAAGTATGGGATGGAGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 610801 | ||||||||||||||||||||
Literature Links: |
SLC41A1 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 |
SLC41A1 - solute carrier family 41 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173854.5 | 2488 | Missense Mutation | CTG,GTG | L,V 485 | NP_776253.3 | |
XM_005245069.2 | 2488 | Missense Mutation | CTG,GTG | L,V 485 | XP_005245126.1 |