Product Details
- SNP ID
-
rs201911810
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:75094868 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCTTACCCCCATGGCACAGTGTAC[A/C]AGCACGCGGCCTGTAGGGAGAACCA
- Phenotype
-
MIM: 613191
MIM: 611575
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
DUSP13
PubMed Links
Gene Details
- Gene
- DUSP13
- Gene Name
- dual specificity phosphatase 13
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001007271.1 |
909 |
UTR 3 |
|
|
NP_001007272.1 |
| NM_001007272.1 |
909 |
Silent Mutation |
CTG,CTT |
L185L |
NP_001007273.1 |
| NM_001007273.1 |
909 |
Silent Mutation |
CTG,CTT |
L228L |
NP_001007274.1 |
| NM_001320842.1 |
909 |
Silent Mutation |
CTG,CTT |
L228L |
NP_001307771.1 |
| NM_001320843.1 |
909 |
Silent Mutation |
CTG,CTT |
L135L |
NP_001307772.1 |
| NM_016364.3 |
909 |
Silent Mutation |
CTG,CTT |
L135L |
NP_057448.3 |
| XM_005269883.3 |
909 |
Silent Mutation |
CTG,CTT |
L354L |
XP_005269940.1 |
| XM_005269884.4 |
909 |
Silent Mutation |
CTG,CTT |
L271L |
XP_005269941.3 |
| XM_005269887.1 |
909 |
Silent Mutation |
CTG,CTT |
L228L |
XP_005269944.1 |
| XM_005269890.1 |
909 |
Silent Mutation |
CTG,CTT |
L135L |
XP_005269947.1 |
| XM_011539853.1 |
909 |
Silent Mutation |
CTG,CTT |
L264L |
XP_011538155.1 |
| XM_011539854.2 |
909 |
Silent Mutation |
CTG,CTT |
L135L |
XP_011538156.1 |
| XM_011539855.1 |
909 |
Silent Mutation |
CTG,CTT |
L135L |
XP_011538157.1 |
| XM_011539856.2 |
909 |
Silent Mutation |
CTG,CTT |
L135L |
XP_011538158.1 |
| XM_017016313.1 |
909 |
Silent Mutation |
CTG,CTT |
L183L |
XP_016871802.1 |
| XM_017016314.1 |
909 |
Intron |
|
|
XP_016871803.1 |
- Gene
- SAMD8
- Gene Name
- sterile alpha motif domain containing 8
There are no transcripts associated with this gene.
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