Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGTTGGCCACGGCCTGCATCCTGC[A/G]CTTGGAGGGCCTGAGGTGTAGAGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 300649 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC38A5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
SLC38A5 - solute carrier family 38 member 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033518.3 | 1040 | Missense Mutation | CGC,TGC | R,C 288 | NP_277053.2 | |
XM_005272694.3 | 1040 | Missense Mutation | CGC,TGC | R,C 335 | XP_005272751.2 | |
XM_005272695.4 | 1040 | Missense Mutation | CGC,TGC | R,C 335 | XP_005272752.3 | |
XM_005272697.2 | 1040 | Missense Mutation | CGC,TGC | R,C 294 | XP_005272754.2 | |
XM_005272698.4 | 1040 | Missense Mutation | CGC,TGC | R,C 288 | XP_005272755.2 | |
XM_006724569.3 | 1040 | Missense Mutation | CGC,TGC | R,C 288 | XP_006724632.1 | |
XM_017029960.1 | 1040 | Missense Mutation | CGC,TGC | R,C 294 | XP_016885449.1 | |
XM_017029961.1 | 1040 | Missense Mutation | CGC,TGC | R,C 288 | XP_016885450.1 |