Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATTTGTTTTCATTGACCAGGTGCC[C/T]GGGAAGAACCCACCGTCCAGCAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
L3MBTL3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
L3MBTL3 - l(3)mbt-like 3 (Drosophila) | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007102.2 | 2131 | Missense Mutation | CGG,TGG | R,W 633 | NP_001007103.1 | |
NM_032438.2 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | NP_115814.1 | |
XM_005267161.4 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_005267218.1 | |
XM_006715576.3 | 2131 | Missense Mutation | CGG,TGG | R,W 693 | XP_006715639.1 | |
XM_006715578.3 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_006715641.1 | |
XM_011536179.2 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_011534481.1 | |
XM_011536180.2 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_011534482.1 | |
XM_011536181.2 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_011534483.1 | |
XM_011536183.2 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_011534485.1 | |
XM_011536184.2 | 2131 | Missense Mutation | CGG,TGG | R,W 658 | XP_011534486.1 | |
XM_017011355.1 | 2131 | Missense Mutation | CGG,TGG | R,W 633 | XP_016866844.1 | |
XM_017011356.1 | 2131 | Missense Mutation | CGG,TGG | R,W 633 | XP_016866845.1 |
SAMD3 - sterile alpha motif domain containing 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017373.3 | 2131 | Intron | NP_001017373.2 | |||
NM_001258275.2 | 2131 | Intron | NP_001245204.1 | |||
NM_001277185.1 | 2131 | Intron | NP_001264114.1 | |||
XM_017010305.1 | 2131 | Intron | XP_016865794.1 | |||
XM_017010306.1 | 2131 | Intron | XP_016865795.1 | |||
XM_017010307.1 | 2131 | Intron | XP_016865796.1 | |||
XM_017010308.1 | 2131 | Intron | XP_016865797.1 | |||
XM_017010309.1 | 2131 | Intron | XP_016865798.1 | |||
XM_017010310.1 | 2131 | Intron | XP_016865799.1 |