Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACCCTGACCACTTCCTCAAGGTCA[G/T]CCTTGGCACAGGCCAGGTGGTTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
10 submissions
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
TTC22 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 |
TTC22 - tetratricopeptide repeat domain 22 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114108.1 | 1217 | Missense Mutation | GAT,GCT | D,A 371 | NP_001107580.1 | |
NM_017904.3 | 1217 | Intron | NP_060374.2 | |||
XM_011541671.2 | 1217 | Intron | XP_011539973.1 | |||
XM_017001582.1 | 1217 | Missense Mutation | GAT,GCT | D,A 180 | XP_016857071.1 |