Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCTTCTGGCTCACAGTGGCTTCTG[C/T]GCTGGTGCTCATCGCGGCCACCATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 104614 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC3A1 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
|
SLC3A1 - solute carrier family 3 member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000341.3 | 368 | Missense Mutation | GCG,GTG | A,V 97 | NP_000332.2 | |
XM_011533047.2 | 368 | Missense Mutation | GCG,GTG | A,V 97 | XP_011531349.1 |