Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCCTGGTGCCAAGTCAGCCGAAC[C/G]ATCACTTCTGCGAGGTACAGCAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610803 | ||||||||||||||||||||
Literature Links: |
SLC41A3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
SLC41A3 - solute carrier family 41 member 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008485.1 | 1432 | Missense Mutation | ATC,ATG | I,M 429 | NP_001008485.1 | |
NM_001008486.1 | 1432 | Missense Mutation | ATC,ATG | I,M 393 | NP_001008486.1 | |
NM_001008487.1 | 1432 | Missense Mutation | ATC,ATG | I,M 403 | NP_001008487.1 | |
NM_001164475.1 | 1432 | Missense Mutation | ATC,ATG | I,M 312 | NP_001157947.1 | |
NM_017836.3 | 1432 | Missense Mutation | ATC,ATG | I,M 429 | NP_060306.3 |