Product Details
- SNP ID
-
rs148873581
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:20165043 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCACATAAAGAATGTTGCTAGGTTT[C/T]AAGTCTCTATGAACCACCTAATTGA
- Phenotype
-
MIM: 300075
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RPS6KA3
PubMed Links
Gene Details
- Gene
- RPS6KA3
- Gene Name
- ribosomal protein S6 kinase A3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004586.2 |
1803 |
Silent Mutation |
TTA,TTG |
L540L |
NP_004577.1 |
XM_005274573.2 |
1803 |
Silent Mutation |
TTA,TTG |
L539L |
XP_005274630.1 |
XM_005274577.2 |
1803 |
Silent Mutation |
TTA,TTG |
L510L |
XP_005274634.1 |
XM_006724507.3 |
1803 |
Silent Mutation |
TTA,TTG |
L511L |
XP_006724570.1 |
XM_011545555.1 |
1803 |
Silent Mutation |
TTA,TTG |
L546L |
XP_011543857.1 |
XM_011545556.1 |
1803 |
Silent Mutation |
TTA,TTG |
L545L |
XP_011543858.1 |
XM_011545557.2 |
1803 |
Silent Mutation |
TTA,TTG |
L518L |
XP_011543859.1 |
XM_011545558.2 |
1803 |
Silent Mutation |
TTA,TTG |
L518L |
XP_011543860.1 |
XM_011545559.1 |
1803 |
Silent Mutation |
TTA,TTG |
L518L |
XP_011543861.1 |
XM_011545560.1 |
1803 |
Silent Mutation |
TTA,TTG |
L518L |
XP_011543862.1 |
XM_011545561.1 |
1803 |
Silent Mutation |
TTA,TTG |
L518L |
XP_011543863.1 |
XM_011545562.1 |
1803 |
Silent Mutation |
TTA,TTG |
L517L |
XP_011543864.1 |
XM_011545563.2 |
1803 |
Silent Mutation |
TTA,TTG |
L512L |
XP_011543865.1 |
XM_017029713.1 |
1803 |
Silent Mutation |
TTA,TTG |
L512L |
XP_016885202.1 |
XM_017029714.1 |
1803 |
Silent Mutation |
TTA,TTG |
L512L |
XP_016885203.1 |
XM_017029715.1 |
1803 |
Silent Mutation |
TTA,TTG |
L512L |
XP_016885204.1 |
XM_017029716.1 |
1803 |
Silent Mutation |
TTA,TTG |
L512L |
XP_016885205.1 |
XM_017029717.1 |
1803 |
Silent Mutation |
TTA,TTG |
L512L |
XP_016885206.1 |
XM_017029718.1 |
1803 |
Silent Mutation |
TTA,TTG |
L511L |
XP_016885207.1 |
XM_017029719.1 |
1803 |
Silent Mutation |
TTA,TTG |
L511L |
XP_016885208.1 |
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