Search
LOADING 
- SNP ID:
- rs201569702
- Gene
-
DMKNKRTDAP - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 35498719 - 35498719 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GTCGGCTCACTCTGACACTCACCTA[C/T]CAAAACTTCACCCACTGCAGCAGGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
DMKN PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| DMKN - dermokine | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001035516.3 | 727 | Nonsense Mutation | TGA,TGG | *,W 90 | NP_001030593.1 | |
| NM_001126056.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 465 | NP_001119528.2 | |
| NM_001126057.2 | 727 | Intron | NP_001119529.2 | |||
| NM_001126058.2 | 727 | Intron | NP_001119530.2 | |||
| NM_001126059.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 189 | NP_001119531.1 | |
| NM_001190347.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 449 | NP_001177276.1 | |
| NM_001190348.1 | 727 | Intron | NP_001177277.1 | |||
| NM_001190349.1 | 727 | Intron | NP_001177278.1 | |||
| NM_001308380.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 203 | NP_001295309.1 | |
| NM_001308383.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 172 | NP_001295312.1 | |
| NM_033317.4 | 727 | Nonsense Mutation | TGA,TGG | *,W 476 | NP_201574.3 | |
| XM_006723477.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 253 | XP_006723540.1 | |
| XM_006723484.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 223 | XP_006723547.1 | |
| XM_006723489.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 184 | XP_006723552.1 | |
| XM_006723493.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 152 | XP_006723556.1 | |
| XM_006723494.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 146 | XP_006723557.1 | |
| XM_006723503.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 184 | XP_006723566.1 | |
| XM_011527494.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 538 | XP_011525796.1 | |
| XM_011527495.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 538 | XP_011525797.1 | |
| XM_011527496.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 526 | XP_011525798.1 | |
| XM_011527497.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 524 | XP_011525799.1 | |
| XM_011527498.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 524 | XP_011525800.1 | |
| XM_011527499.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 523 | XP_011525801.1 | |
| XM_011527500.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 520 | XP_011525802.1 | |
| XM_011527501.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 518 | XP_011525803.1 | |
| XM_011527502.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 508 | XP_011525804.1 | |
| XM_011527503.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 506 | XP_011525805.1 | |
| XM_011527504.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 500 | XP_011525806.1 | |
| XM_011527505.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 491 | XP_011525807.1 | |
| XM_011527506.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 488 | XP_011525808.1 | |
| XM_011527507.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 476 | XP_011525809.1 | |
| XM_011527508.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 471 | XP_011525810.1 | |
| XM_011527509.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 457 | XP_011525811.1 | |
| XM_011527510.2 | 727 | Nonsense Mutation | TGA,TGG | *,W 456 | XP_011525812.1 | |
| XM_011527511.2 | 727 | Intron | XP_011525813.1 | |||
| XM_011527512.2 | 727 | Intron | XP_011525814.1 | |||
| XM_011527513.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 206 | XP_011525815.1 | |
| XM_011527514.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 186 | XP_011525816.1 | |
| XM_017027475.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 221 | XP_016882964.1 | |
| XM_017027476.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 184 | XP_016882965.1 | |
| XM_017027477.1 | 727 | Nonsense Mutation | TGA,TGG | *,W 137 | XP_016882966.1 | |
| KRTDAP - keratinocyte differentiation associated protein | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To Top