Product Details
- SNP ID
-
rs142000561
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:35498897 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCGAGGAAGAAGGTGAGACTCCCC[C/G]CTGCAAAAAGATCAAAGGAAAGTGA
- Phenotype
-
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
DMKN
PubMed Links
Gene Details
- Gene
- DMKN
- Gene Name
- dermokine
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001035516.3 |
659 |
Missense Mutation |
CGG,GGG |
R68G |
NP_001030593.1 |
NM_001126056.2 |
659 |
Missense Mutation |
CGG,GGG |
R443G |
NP_001119528.2 |
NM_001126057.2 |
659 |
Intron |
|
|
NP_001119529.2 |
NM_001126058.2 |
659 |
Intron |
|
|
NP_001119530.2 |
NM_001126059.2 |
659 |
Missense Mutation |
CGG,GGG |
R167G |
NP_001119531.1 |
NM_001190347.1 |
659 |
Missense Mutation |
CGG,GGG |
R427G |
NP_001177276.1 |
NM_001190348.1 |
659 |
Intron |
|
|
NP_001177277.1 |
NM_001190349.1 |
659 |
Intron |
|
|
NP_001177278.1 |
NM_001308380.1 |
659 |
Missense Mutation |
CGG,GGG |
R181G |
NP_001295309.1 |
NM_001308383.1 |
659 |
Missense Mutation |
CGG,GGG |
R150G |
NP_001295312.1 |
NM_033317.4 |
659 |
Missense Mutation |
CGG,GGG |
R454G |
NP_201574.3 |
XM_006723477.1 |
659 |
Missense Mutation |
CGG,GGG |
R231G |
XP_006723540.1 |
XM_006723484.1 |
659 |
Missense Mutation |
CGG,GGG |
R201G |
XP_006723547.1 |
XM_006723489.1 |
659 |
Missense Mutation |
CGG,GGG |
R162G |
XP_006723552.1 |
XM_006723493.2 |
659 |
Missense Mutation |
CGG,GGG |
R130G |
XP_006723556.1 |
XM_006723494.2 |
659 |
Missense Mutation |
CGG,GGG |
R124G |
XP_006723557.1 |
XM_006723503.2 |
659 |
Missense Mutation |
CGG,GGG |
R162G |
XP_006723566.1 |
XM_011527494.2 |
659 |
Missense Mutation |
CGG,GGG |
R516G |
XP_011525796.1 |
XM_011527495.2 |
659 |
Missense Mutation |
CGG,GGG |
R516G |
XP_011525797.1 |
XM_011527496.2 |
659 |
Missense Mutation |
CGG,GGG |
R504G |
XP_011525798.1 |
XM_011527497.2 |
659 |
Missense Mutation |
CGG,GGG |
R502G |
XP_011525799.1 |
XM_011527498.2 |
659 |
Missense Mutation |
CGG,GGG |
R502G |
XP_011525800.1 |
XM_011527499.2 |
659 |
Missense Mutation |
CGG,GGG |
R501G |
XP_011525801.1 |
XM_011527500.2 |
659 |
Missense Mutation |
CGG,GGG |
R498G |
XP_011525802.1 |
XM_011527501.2 |
659 |
Missense Mutation |
CGG,GGG |
R496G |
XP_011525803.1 |
XM_011527502.2 |
659 |
Missense Mutation |
CGG,GGG |
R486G |
XP_011525804.1 |
XM_011527503.2 |
659 |
Missense Mutation |
CGG,GGG |
R484G |
XP_011525805.1 |
XM_011527504.2 |
659 |
Missense Mutation |
CGG,GGG |
R478G |
XP_011525806.1 |
XM_011527505.2 |
659 |
Missense Mutation |
CGG,GGG |
R469G |
XP_011525807.1 |
XM_011527506.2 |
659 |
Missense Mutation |
CGG,GGG |
R466G |
XP_011525808.1 |
XM_011527507.2 |
659 |
Missense Mutation |
CGG,GGG |
R454G |
XP_011525809.1 |
XM_011527508.2 |
659 |
Missense Mutation |
CGG,GGG |
R449G |
XP_011525810.1 |
XM_011527509.2 |
659 |
Missense Mutation |
CGG,GGG |
R435G |
XP_011525811.1 |
XM_011527510.2 |
659 |
Missense Mutation |
CGG,GGG |
R434G |
XP_011525812.1 |
XM_011527511.2 |
659 |
Intron |
|
|
XP_011525813.1 |
XM_011527512.2 |
659 |
Intron |
|
|
XP_011525814.1 |
XM_011527513.1 |
659 |
Missense Mutation |
CGG,GGG |
R184G |
XP_011525815.1 |
XM_011527514.1 |
659 |
Missense Mutation |
CGG,GGG |
R164G |
XP_011525816.1 |
XM_017027475.1 |
659 |
Missense Mutation |
CGG,GGG |
R199G |
XP_016882964.1 |
XM_017027476.1 |
659 |
Missense Mutation |
CGG,GGG |
R162G |
XP_016882965.1 |
XM_017027477.1 |
659 |
Missense Mutation |
CGG,GGG |
R115G |
XP_016882966.1 |
- Gene
- KRTDAP
- Gene Name
- keratinocyte differentiation associated protein
There are no transcripts associated with this gene.
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