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Search Thermo Fisher Scientific
ATTCAGGGTGGGGACGCAGTTCCTG[C/T]CGTGGCTGTCCTTTGAGAGACCCAC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609699 | |||||||||||||||||||||||
Literature Links: |
MGLL PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
MGLL - monoglyceride lipase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003794.2 | 1206 | Missense Mutation | ACA,GCA | T,A 297 | NP_001003794.1 | |
NM_001256585.1 | 1206 | Missense Mutation | ACA,GCA | T,A 277 | NP_001243514.1 | |
NM_007283.6 | 1206 | Missense Mutation | ACA,GCA | T,A 307 | NP_009214.1 | |
XM_011512377.1 | 1206 | Missense Mutation | ACA,GCA | T,A 333 | XP_011510679.1 | |
XM_011512378.1 | 1206 | Missense Mutation | ACA,GCA | T,A 323 | XP_011510680.1 | |
XM_011512379.2 | 1206 | Missense Mutation | ACA,GCA | T,A 297 | XP_011510681.1 | |
XM_011512382.1 | 1206 | Missense Mutation | ACA,GCA | T,A 260 | XP_011510684.1 | |
XM_011512383.2 | 1206 | Missense Mutation | ACA,GCA | T,A 241 | XP_011510685.1 | |
XM_017005662.1 | 1206 | Intron | XP_016861151.1 | |||
XM_017005663.1 | 1206 | Intron | XP_016861152.1 | |||
XM_017005664.1 | 1206 | Missense Mutation | ACA,GCA | T,A 271 | XP_016861153.1 | |
XM_017005665.1 | 1206 | Missense Mutation | ACA,GCA | T,A 271 | XP_016861154.1 | |
XM_017005666.1 | 1206 | Missense Mutation | ACA,GCA | T,A 267 | XP_016861155.1 |