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Search Thermo Fisher Scientific
CCTAGGATAAATGTCACCGAAGATA[C/T]GGCCCAAAAGCTGGACACGAGCCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616203 | ||||||||||||||||||||
Literature Links: |
SLC38A9 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 |
SLC38A9 - solute carrier family 38 member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258286.1 | 1829 | Missense Mutation | CAT,CGT | H,R 406 | NP_001245215.1 | |
NM_001258287.1 | 1829 | Missense Mutation | CAT,CGT | H,R 406 | NP_001245216.1 | |
NM_001282429.1 | 1829 | Missense Mutation | CAT,CGT | H,R 345 | NP_001269358.1 | |
NM_173514.3 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | NP_775785.2 | |
XM_006714537.2 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_006714600.1 | |
XM_006714538.3 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_006714601.1 | |
XM_006714539.3 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_006714602.1 | |
XM_011543173.1 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_011541475.1 | |
XM_011543174.1 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_011541476.1 | |
XM_011543176.1 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_011541478.1 | |
XM_011543177.1 | 1829 | Missense Mutation | CAT,CGT | H,R 433 | XP_011541479.1 | |
XM_011543178.1 | 1829 | Missense Mutation | CAT,CGT | H,R 412 | XP_011541480.1 | |
XM_011543180.1 | 1829 | Missense Mutation | CAT,CGT | H,R 368 | XP_011541482.1 | |
XM_011543182.1 | 1829 | Silent Mutation | CCA,CCG | P,P 452 | XP_011541484.1 | |
XM_011543183.1 | 1829 | Missense Mutation | CAT,CGT | H,R 347 | XP_011541485.1 | |
XM_011543184.1 | 1829 | Missense Mutation | CAT,CGT | H,R 311 | XP_011541486.1 | |
XM_017009077.1 | 1829 | Missense Mutation | CAT,CGT | H,R 469 | XP_016864566.1 | |
XM_017009078.1 | 1829 | Missense Mutation | CAT,CGT | H,R 412 | XP_016864567.1 | |
XM_017009079.1 | 1829 | Missense Mutation | CAT,CGT | H,R 404 | XP_016864568.1 | |
XM_017009080.1 | 1829 | Missense Mutation | CAT,CGT | H,R 404 | XP_016864569.1 | |
XM_017009081.1 | 1829 | Missense Mutation | CAT,CGT | H,R 404 | XP_016864570.1 | |
XM_017009082.1 | 1829 | Missense Mutation | CAT,CGT | H,R 368 | XP_016864571.1 |