Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCATTTTAAGTAGTTATGAAGAAAC[A/T]CGCTTGTAATGAAATTGCAAAAGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LMNTD1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
LMNTD1 - lamin tail domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145727.2 | Intron | NP_001139199.1 | ||||
NM_001145728.2 | Intron | NP_001139200.1 | ||||
NM_001145729.1 | Intron | NP_001139201.1 | ||||
NM_001256266.1 | Intron | NP_001243195.1 | ||||
NM_152590.3 | Intron | NP_689803.2 | ||||
XM_011520575.1 | Intron | XP_011518877.1 | ||||
XM_011520576.2 | Intron | XP_011518878.1 | ||||
XM_011520577.2 | Intron | XP_011518879.1 | ||||
XM_011520578.2 | Intron | XP_011518880.1 | ||||
XM_011520579.2 | Intron | XP_011518881.1 | ||||
XM_011520580.1 | Intron | XP_011518882.1 | ||||
XM_011520582.1 | Intron | XP_011518884.1 | ||||
XM_011520583.1 | Intron | XP_011518885.1 | ||||
XM_011520584.1 | Intron | XP_011518886.1 | ||||
XM_011520585.2 | Intron | XP_011518887.1 | ||||
XM_011520587.1 | Intron | XP_011518889.1 | ||||
XM_011520588.1 | Intron | XP_011518890.1 | ||||
XM_017018891.1 | Intron | XP_016874380.1 | ||||
XM_017018892.1 | Intron | XP_016874381.1 | ||||
XM_017018893.1 | Intron | XP_016874382.1 | ||||
XM_017018894.1 | Intron | XP_016874383.1 | ||||
XM_017018895.1 | Intron | XP_016874384.1 |