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GGAGAGCTGCAGCCTCACCACGCCC[C/T]GGGGGTCCCTTCCCTGCTTTGTAGG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZDHHC19 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 - 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 |
ZDHHC19 - zinc finger DHHC-type containing 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039617.1 | 1011 | Missense Mutation | AGG,GGG | R,G 307 | NP_001034706.1 | |
XM_005269279.2 | 1011 | Intron | XP_005269336.1 | |||
XM_006713493.2 | 1011 | Missense Mutation | AGG,GGG | R,G 305 | XP_006713556.1 | |
XM_006713494.2 | 1011 | Missense Mutation | AGG,GGG | R,G 281 | XP_006713557.1 | |
XM_011512417.1 | 1011 | Missense Mutation | AGG,GGG | R,G 233 | XP_011510719.1 |