Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATCATGACTTCTTACCTTTCTAGC[A/T]GCATTTTCTTTTCTGCTATTAGGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 614394 MIM: 612912 MIM: 191161 | ||||||||||||||||||||
Literature Links: |
IFT20 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 |
IFT20 - intraflagellar transport 20 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267774.1 | 460 | Missense Mutation | CAG,CTG | Q,L 129 | NP_001254703.1 | |
NM_001267775.1 | 460 | Missense Mutation | CAG,CTG | Q,L 103 | NP_001254704.1 | |
NM_001267776.1 | 460 | Missense Mutation | CAG,CTG | Q,L 103 | NP_001254705.1 | |
NM_001267777.1 | 460 | Missense Mutation | CAG,CTG | Q,L 103 | NP_001254706.1 | |
NM_001267778.1 | 460 | Intron | NP_001254707.1 | |||
NM_174887.3 | 460 | Silent Mutation | GCA,GCT | A,A 142 | NP_777547.1 |
TMEM97 - transmembrane protein 97 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014573.2 | 460 | Intron | NP_055388.2 | |||
XM_005257965.3 | 460 | Intron | XP_005258022.1 |
TNFAIP1 - TNF alpha induced protein 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |