Product Details
- SNP ID
-
rs201885024
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:90873741 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGACTTCCATCTTGTAGCCATTCA[C/T]TGTACCTCAAGCCAGACATTTTAAG
- Phenotype
-
MIM: 603607
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RPS6KA5
PubMed Links
Gene Details
- Gene
- RPS6KA5
- Gene Name
- ribosomal protein S6 kinase A5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001322227.1 |
2158 |
Missense Mutation |
AAT,AGT |
N403S |
NP_001309156.1 |
NM_001322228.1 |
2158 |
Missense Mutation |
AAT,AGT |
N648S |
NP_001309157.1 |
NM_001322229.1 |
2158 |
Missense Mutation |
AAT,AGT |
N677S |
NP_001309158.1 |
NM_001322230.1 |
2158 |
Missense Mutation |
AAT,AGT |
N417S |
NP_001309159.1 |
NM_001322231.1 |
2158 |
Missense Mutation |
AAT,AGT |
N445S |
NP_001309160.1 |
NM_001322232.1 |
2158 |
Missense Mutation |
AAT,AGT |
N611S |
NP_001309161.1 |
NM_001322233.1 |
2158 |
Missense Mutation |
AAT,AGT |
N630S |
NP_001309162.1 |
NM_001322234.1 |
2158 |
Missense Mutation |
AAT,AGT |
N492S |
NP_001309163.1 |
NM_001322235.1 |
2158 |
Missense Mutation |
AAT,AGT |
N605S |
NP_001309164.1 |
NM_001322236.1 |
2158 |
Missense Mutation |
AAT,AGT |
N656S |
NP_001309165.1 |
NM_001322237.1 |
2158 |
Missense Mutation |
AAT,AGT |
N605S |
NP_001309166.1 |
NM_001322238.1 |
2158 |
Missense Mutation |
AAT,AGT |
N465S |
NP_001309167.1 |
NM_004755.3 |
2158 |
Missense Mutation |
AAT,AGT |
N684S |
NP_004746.2 |
NM_182398.2 |
2158 |
Intron |
|
|
NP_872198.1 |
XM_017021786.1 |
2158 |
Missense Mutation |
AAT,AGT |
N465S |
XP_016877275.1 |
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