Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGACAGAGACTCACCTGATCGTCT[A/C]TGCCTGCACGTTTCTGCAGTGATGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DMKN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
DMKN - dermokine | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001035516.3 | 534 | Missense Mutation | AGA,ATA | R,I 40 | NP_001030593.1 | |
NM_001126056.2 | 534 | Missense Mutation | AGA,ATA | R,I 415 | NP_001119528.2 | |
NM_001126057.2 | 534 | Intron | NP_001119529.2 | |||
NM_001126058.2 | 534 | Intron | NP_001119530.2 | |||
NM_001126059.2 | 534 | Missense Mutation | AGA,ATA | R,I 139 | NP_001119531.1 | |
NM_001190347.1 | 534 | Missense Mutation | AGA,ATA | R,I 385 | NP_001177276.1 | |
NM_001190348.1 | 534 | Intron | NP_001177277.1 | |||
NM_001190349.1 | 534 | Intron | NP_001177278.1 | |||
NM_001308380.1 | 534 | Missense Mutation | AGA,ATA | R,I 139 | NP_001295309.1 | |
NM_001308383.1 | 534 | Missense Mutation | AGA,ATA | R,I 122 | NP_001295312.1 | |
NM_033317.4 | 534 | Missense Mutation | AGA,ATA | R,I 426 | NP_201574.3 | |
XM_006723477.1 | 534 | Missense Mutation | AGA,ATA | R,I 189 | XP_006723540.1 | |
XM_006723484.1 | 534 | Missense Mutation | AGA,ATA | R,I 159 | XP_006723547.1 | |
XM_006723489.1 | 534 | Missense Mutation | AGA,ATA | R,I 120 | XP_006723552.1 | |
XM_006723493.2 | 534 | Missense Mutation | AGA,ATA | R,I 102 | XP_006723556.1 | |
XM_006723494.2 | 534 | Missense Mutation | AGA,ATA | R,I 82 | XP_006723557.1 | |
XM_006723503.2 | 534 | Missense Mutation | AGA,ATA | R,I 120 | XP_006723566.1 | |
XM_011527494.2 | 534 | Missense Mutation | AGA,ATA | R,I 474 | XP_011525796.1 | |
XM_011527495.2 | 534 | Missense Mutation | AGA,ATA | R,I 474 | XP_011525797.1 | |
XM_011527496.2 | 534 | Missense Mutation | AGA,ATA | R,I 462 | XP_011525798.1 | |
XM_011527497.2 | 534 | Missense Mutation | AGA,ATA | R,I 474 | XP_011525799.1 | |
XM_011527498.2 | 534 | Missense Mutation | AGA,ATA | R,I 474 | XP_011525800.1 | |
XM_011527499.2 | 534 | Missense Mutation | AGA,ATA | R,I 459 | XP_011525801.1 | |
XM_011527500.2 | 534 | Missense Mutation | AGA,ATA | R,I 456 | XP_011525802.1 | |
XM_011527501.2 | 534 | Missense Mutation | AGA,ATA | R,I 454 | XP_011525803.1 | |
XM_011527502.2 | 534 | Missense Mutation | AGA,ATA | R,I 444 | XP_011525804.1 | |
XM_011527503.2 | 534 | Missense Mutation | AGA,ATA | R,I 442 | XP_011525805.1 | |
XM_011527504.2 | 534 | Missense Mutation | AGA,ATA | R,I 436 | XP_011525806.1 | |
XM_011527505.2 | 534 | Missense Mutation | AGA,ATA | R,I 427 | XP_011525807.1 | |
XM_011527506.2 | 534 | Missense Mutation | AGA,ATA | R,I 424 | XP_011525808.1 | |
XM_011527507.2 | 534 | Missense Mutation | AGA,ATA | R,I 412 | XP_011525809.1 | |
XM_011527508.2 | 534 | Missense Mutation | AGA,ATA | R,I 407 | XP_011525810.1 | |
XM_011527509.2 | 534 | Missense Mutation | AGA,ATA | R,I 407 | XP_011525811.1 | |
XM_011527510.2 | 534 | Missense Mutation | AGA,ATA | R,I 392 | XP_011525812.1 | |
XM_011527511.2 | 534 | Intron | XP_011525813.1 | |||
XM_011527512.2 | 534 | Intron | XP_011525814.1 | |||
XM_011527513.1 | 534 | Missense Mutation | AGA,ATA | R,I 142 | XP_011525815.1 | |
XM_011527514.1 | 534 | Missense Mutation | AGA,ATA | R,I 122 | XP_011525816.1 | |
XM_017027475.1 | 534 | Missense Mutation | AGA,ATA | R,I 157 | XP_016882964.1 | |
XM_017027476.1 | 534 | Missense Mutation | AGA,ATA | R,I 120 | XP_016882965.1 | |
XM_017027477.1 | 534 | Missense Mutation | AGA,ATA | R,I 73 | XP_016882966.1 |