Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTATTTACTCCCTCATTTTCCACA[A/T]CCTGGATGCTGTCAAGAAGAGGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 610792 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A25 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
|
SLC22A25 - solute carrier family 22 member 25 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_199352.3 | 1715 | Missense Mutation | GAT,GTT | D,V 529 | NP_955384.3 | |
XM_017017684.1 | 1715 | Missense Mutation | GAT,GTT | D,V 559 | XP_016873173.1 | |
XM_017017685.1 | 1715 | Missense Mutation | GAT,GTT | D,V 559 | XP_016873174.1 | |
XM_017017686.1 | 1715 | Missense Mutation | GAT,GTT | D,V 559 | XP_016873175.1 | |
XM_017017687.1 | 1715 | Missense Mutation | GAT,GTT | D,V 529 | XP_016873176.1 | |
XM_017017688.1 | 1715 | Missense Mutation | GAT,GTT | D,V 459 | XP_016873177.1 | |
XM_017017689.1 | 1715 | Missense Mutation | GAT,GTT | D,V 448 | XP_016873178.1 | |
XM_017017690.1 | 1715 | Missense Mutation | GAT,GTT | D,V 434 | XP_016873179.1 | |
XM_017017691.1 | 1715 | Missense Mutation | GAT,GTT | D,V 434 | XP_016873180.1 | |
XM_017017692.1 | 1715 | Missense Mutation | GAT,GTT | D,V 387 | XP_016873181.1 | |
XM_017017693.1 | 1715 | Missense Mutation | GAT,GTT | D,V 363 | XP_016873182.1 | |
XM_017017694.1 | 1715 | Missense Mutation | GAT,GTT | D,V 361 | XP_016873183.1 | |
XM_017017695.1 | 1715 | Intron | XP_016873184.1 | |||
XM_017017696.1 | 1715 | Missense Mutation | GAT,GTT | D,V 298 | XP_016873185.1 |