Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCATTTACCCACCAGGTCCTCATCC[A/G]GCCTCAGGTGCACCTTCTTCATCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616567 | ||||||||||||||||||||
Literature Links: |
DAPK2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
DAPK2 - death associated protein kinase 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014326.3 | 1025 | Missense Mutation | CCG,CTG | P,L 340 | NP_055141.2 | |
XM_011521413.2 | 1025 | Missense Mutation | CCG,CTG | P,L 340 | XP_011519715.1 | |
XM_011521414.1 | 1025 | Missense Mutation | CCG,CTG | P,L 340 | XP_011519716.1 | |
XM_011521415.2 | 1025 | Intron | XP_011519717.1 | |||
XM_011521416.2 | 1025 | Intron | XP_011519718.1 | |||
XM_011521417.1 | 1025 | UTR 3 | XP_011519719.1 | |||
XM_011521421.2 | 1025 | Missense Mutation | CCG,CTG | P,L 185 | XP_011519723.1 | |
XM_017022043.1 | 1025 | Intron | XP_016877532.1 | |||
XM_017022044.1 | 1025 | Missense Mutation | CCG,CTG | P,L 340 | XP_016877533.1 | |
XM_017022045.1 | 1025 | UTR 3 | XP_016877534.1 | |||
XM_017022046.1 | 1025 | UTR 3 | XP_016877535.1 | |||
XM_017022047.1 | 1025 | Intron | XP_016877536.1 | |||
XM_017022048.1 | 1025 | Intron | XP_016877537.1 | |||
XM_017022049.1 | 1025 | Intron | XP_016877538.1 | |||
XM_017022050.1 | 1025 | Intron | XP_016877539.1 | |||
XM_017022051.1 | 1025 | Intron | XP_016877540.1 | |||
XM_017022052.1 | 1025 | Intron | XP_016877541.1 |