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GAAATGTGAAAACTGCTATGTTTCC[A/G]TTTCCACAGCAAGAGATGATGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300576 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZDHHC15 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZDHHC15 - zinc finger DHHC-type containing 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146256.1 | 1455 | Missense Mutation | ACG,ATG | T,M 326 | NP_001139728.1 | |
NM_001146257.1 | 1455 | Intron | NP_001139729.1 | |||
NM_144969.2 | 1455 | Missense Mutation | ACG,ATG | T,M 335 | NP_659406.1 | |
XM_006724624.3 | 1455 | Missense Mutation | ACG,ATG | T,M 335 | XP_006724687.1 | |
XM_017029296.1 | 1455 | Intron | XP_016884785.1 | |||
XM_017029297.1 | 1455 | Missense Mutation | ACG,ATG | T,M 186 | XP_016884786.1 | |
XM_017029298.1 | 1455 | Intron | XP_016884787.1 |