Product Details
- SNP ID
-
rs144181389
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:99399114 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGAAAGATCGTGGTTTTTCAAGAC[A/G]GATTTATCTTCCTGGAAAACAAGAG
- Phenotype
-
MIM: 615671
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SETD3
PubMed Links
Gene Details
- Gene
- SETD3
- Gene Name
- SET domain containing 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_032233.2 |
1368 |
Silent Mutation |
TCC,TCT |
S450S |
NP_115609.2 |
NM_199123.1 |
1368 |
Intron |
|
|
NP_954574.1 |
XM_005268127.3 |
1368 |
Silent Mutation |
TCC,TCT |
S351S |
XP_005268184.1 |
XM_011537231.2 |
1368 |
Silent Mutation |
TCC,TCT |
S450S |
XP_011535533.2 |
XM_011537232.2 |
1368 |
Silent Mutation |
TCC,TCT |
S450S |
XP_011535534.1 |
XM_011537233.2 |
1368 |
Silent Mutation |
TCC,TCT |
S392S |
XP_011535535.1 |
XM_011537234.1 |
1368 |
Silent Mutation |
TCC,TCT |
S351S |
XP_011535536.1 |
XM_011537235.1 |
1368 |
Intron |
|
|
XP_011535537.1 |
XM_017021699.1 |
1368 |
Silent Mutation |
TCC,TCT |
S450S |
XP_016877188.1 |
XM_017021700.1 |
1368 |
Silent Mutation |
TCC,TCT |
S450S |
XP_016877189.1 |
XM_017021701.1 |
1368 |
Silent Mutation |
TCC,TCT |
S392S |
XP_016877190.1 |
XM_017021702.1 |
1368 |
Silent Mutation |
TCC,TCT |
S293S |
XP_016877191.1 |
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