Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGAGGGTGTGGACACCCAGTGATG[C/T]TGTTCTCAACCAGCCATTGAGGATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
CNOT6L 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 |
CNOT6L - CCR4-NOT transcription complex subunit 6 like | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286790.1 | 1655 | Missense Mutation | AAC,AGC | N,S 516 | NP_001273719.1 | |
NM_144571.2 | 1655 | Missense Mutation | AAC,AGC | N,S 516 | NP_653172.2 | |
XM_011531806.2 | 1655 | Missense Mutation | AAC,AGC | N,S 563 | XP_011530108.1 | |
XM_011531807.2 | 1655 | Missense Mutation | AAC,AGC | N,S 555 | XP_011530109.1 | |
XM_011531808.2 | 1655 | Missense Mutation | AAC,AGC | N,S 524 | XP_011530110.1 | |
XM_011531809.1 | 1655 | Missense Mutation | AAC,AGC | N,S 524 | XP_011530111.1 | |
XM_011531810.1 | 1655 | Missense Mutation | AAC,AGC | N,S 519 | XP_011530112.1 | |
XM_017007956.1 | 1655 | Missense Mutation | AAC,AGC | N,S 519 | XP_016863445.1 | |
XM_017007957.1 | 1655 | Missense Mutation | AAC,AGC | N,S 511 | XP_016863446.1 |