Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAAGTAGGCTCCGATCCTCTTCCG[A/C]ACCCACCACTTGCCCTCGGCGGCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 611761 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LMF1 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
|
LMF1 - lipase maturation factor 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022773.2 | 2191 | Silent Mutation | GTG,GTT | V,V 536 | NP_073610.2 | |
XM_006720928.2 | 2191 | Silent Mutation | GTG,GTT | V,V 427 | XP_006720991.1 | |
XM_006720929.3 | 2191 | Silent Mutation | GTG,GTT | V,V 403 | XP_006720992.1 | |
XM_011522614.2 | 2191 | Intron | XP_011520916.1 | |||
XM_011522615.1 | 2191 | Intron | XP_011520917.1 | |||
XM_011522617.2 | 2191 | Silent Mutation | GTG,GTT | V,V 319 | XP_011520919.1 | |
XM_011522618.2 | 2191 | Intron | XP_011520920.1 | |||
XM_017023575.1 | 2191 | Intron | XP_016879064.1 | |||
XM_017023576.1 | 2191 | Silent Mutation | GTG,GTT | V,V 458 | XP_016879065.1 | |
XM_017023577.1 | 2191 | Silent Mutation | GTG,GTT | V,V 403 | XP_016879066.1 | |
XM_017023578.1 | 2191 | Silent Mutation | GTG,GTT | V,V 324 | XP_016879067.1 | |
XM_017023579.1 | 2191 | Silent Mutation | GTG,GTT | V,V 319 | XP_016879068.1 | |
XM_017023580.1 | 2191 | Silent Mutation | GTG,GTT | V,V 319 | XP_016879069.1 | |
XM_017023581.1 | 2191 | Intron | XP_016879070.1 |