Product Details
- SNP ID
-
rs201095031
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:141136720 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGGGCCTCCCGGGGCCCCCCAGAG[C/T]GCCAGAGCCTGAGGATGTCGCCGTC
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DENND3
PubMed Links
Gene Details
- Gene
- DENND3
- Gene Name
- DENN domain containing 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_014957.2 |
338 |
Missense Mutation |
GCG,GTG |
A25V |
NP_055772.2 |
XM_005250838.4 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_005250895.2 |
XM_005250839.2 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_005250896.2 |
XM_005250840.4 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_005250897.2 |
XM_005250841.3 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_005250898.2 |
XM_005250842.4 |
338 |
Missense Mutation |
GCG,GTG |
A105V |
XP_005250899.1 |
XM_011516933.1 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515235.1 |
XM_011516934.2 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515236.1 |
XM_011516937.1 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515239.1 |
XM_011516938.2 |
338 |
Intron |
|
|
XP_011515240.1 |
XM_011516939.2 |
338 |
Intron |
|
|
XP_011515241.1 |
XM_011516940.2 |
338 |
Intron |
|
|
XP_011515242.1 |
XM_011516941.2 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_011515243.1 |
XM_017013241.1 |
338 |
Missense Mutation |
GCG,GTG |
A38V |
XP_016868730.1 |
XM_017013242.1 |
338 |
UTR 5 |
|
|
XP_016868731.1 |
XM_017013243.1 |
338 |
Intron |
|
|
XP_016868732.1 |
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