Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCTTCAGAGTTCCCCCAACTCGG[A/G]GGCTGTCCGGCCCTTTTATGCCTCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
CCDC60 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 |
CCDC60 - coiled-coil domain containing 60 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178499.4 | 298 | Missense Mutation | GAG,GGG | E,G 17 | NP_848594.2 | |
XM_017018911.1 | 298 | Missense Mutation | GAG,GGG | E,G 17 | XP_016874400.1 | |
XM_017018912.1 | 298 | Missense Mutation | GAG,GGG | E,G 17 | XP_016874401.1 | |
XM_017018913.1 | 298 | Missense Mutation | GAG,GGG | E,G 17 | XP_016874402.1 | |
XM_017018914.1 | 298 | Intron | XP_016874403.1 | |||
XM_017018915.1 | 298 | Intron | XP_016874404.1 | |||
XM_017018916.1 | 298 | Intron | XP_016874405.1 |