Product Details

SNP ID
rs11048065
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:25483123 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGACAAAGAGCAGAGACTAAAATGG[A/T]TATAAGAAGTCTTAATGTGGGCTGG
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
LMNTD1 PubMed Links

Gene Details

Gene
LMNTD1
Gene Name
lamin tail domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change 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

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