Product Details
- SNP ID
-
rs144434999
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:128074990 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAACACCAAGTGAATTAGTGAACAC[C/T]GGAGTGAGTATTGTTTTAAAGTTTT
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
LARP1B
PubMed Links
Gene Details
- Gene
- LARP1B
- Gene Name
- La ribonucleoprotein domain family member 1B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001278604.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
NP_001265533.1 |
NM_018078.3 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
NP_060548.2 |
NM_032239.3 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
NP_115615.2 |
NM_178043.2 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
NP_835144.1 |
XM_011532057.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530359.2 |
XM_011532058.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530360.2 |
XM_011532059.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530361.2 |
XM_011532060.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530362.2 |
XM_011532061.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530363.1 |
XM_011532062.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530364.2 |
XM_011532063.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530365.2 |
XM_011532064.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530366.2 |
XM_011532065.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530367.1 |
XM_011532067.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_011530369.1 |
XM_011532068.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_011530370.1 |
XM_011532069.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_011530371.1 |
XM_011532070.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530372.2 |
XM_011532072.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530374.2 |
XM_011532073.2 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_011530375.2 |
XM_011532075.1 |
1044 |
UTR 5 |
|
|
XP_011530377.1 |
XM_011532076.2 |
1044 |
Intron |
|
|
XP_011530378.1 |
XM_011532077.2 |
1044 |
Intron |
|
|
XP_011530379.1 |
XM_017008338.1 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_016863827.1 |
XM_017008339.1 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_016863828.1 |
XM_017008340.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_016863829.1 |
XM_017008341.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_016863830.1 |
XM_017008342.1 |
1044 |
Intron |
|
|
XP_016863831.1 |
XM_017008343.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_016863832.1 |
XM_017008344.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_016863833.1 |
XM_017008345.1 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_016863834.1 |
XM_017008346.1 |
1044 |
Intron |
|
|
XP_016863835.1 |
XM_017008347.1 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_016863836.1 |
XM_017008348.1 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_016863837.1 |
XM_017008349.1 |
1044 |
Intron |
|
|
XP_016863838.1 |
XM_017008350.1 |
1044 |
Intron |
|
|
XP_016863839.1 |
XM_017008351.1 |
1044 |
UTR 5 |
|
|
XP_016863840.1 |
XM_017008352.1 |
1044 |
Silent Mutation |
ACC,ACT |
T214T |
XP_016863841.1 |
XM_017008353.1 |
1044 |
Silent Mutation |
ACC,ACT |
T13T |
XP_016863842.1 |
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