Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATTGCTGTGAACTCCAGCCAAGAT[A/G]GTGTGGTTGAGGGAGGAAGCCGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 602282 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LPAR1 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
|
LPAR1 - lysophosphatidic acid receptor 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001401.3 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | NP_001392.2 | |
NM_057159.2 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | NP_476500.1 | |
XM_005251781.3 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_005251838.1 | |
XM_005251782.3 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_005251839.1 | |
XM_017014383.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869872.1 | |
XM_017014384.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869873.1 | |
XM_017014385.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869874.1 | |
XM_017014386.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869875.1 | |
XM_017014387.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869876.1 | |
XM_017014388.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869877.1 | |
XM_017014389.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869878.1 | |
XM_017014390.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869879.1 | |
XM_017014391.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869880.1 | |
XM_017014392.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869881.1 | |
XM_017014393.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869882.1 | |
XM_017014394.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869883.1 | |
XM_017014395.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869884.1 | |
XM_017014396.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869885.1 | |
XM_017014397.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869886.1 | |
XM_017014398.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869887.1 | |
XM_017014399.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869888.1 | |
XM_017014400.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869889.1 | |
XM_017014401.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869890.1 | |
XM_017014402.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869891.1 | |
XM_017014403.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869892.1 | |
XM_017014404.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869893.1 | |
XM_017014405.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869894.1 | |
XM_017014406.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869895.1 | |
XM_017014407.1 | 1437 | Silent Mutation | ACC,ACT | T,T 351 | XP_016869896.1 |