Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGCGCGTGCCCTCAGCTGCTGGC[G/A]AGGGACTGGTGGATGGGCGGCTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 606322 MIM: 608146 | ||||||||||||||||||||
Literature Links: |
CYFIP1 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 |
CYFIP1 - cytoplasmic FMR1 interacting protein 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033028.1 | 4293 | Silent Mutation | CTC,CTT | L,L 819 | NP_001028200.1 | |
NM_001287810.2 | 4293 | Silent Mutation | CTC,CTT | L,L 1250 | NP_001274739.1 | |
NM_001324119.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1284 | NP_001311048.1 | |
NM_001324120.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1250 | NP_001311049.1 | |
NM_001324122.1 | 4293 | Silent Mutation | CTC,CTT | L,L 690 | NP_001311051.1 | |
NM_001324123.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1250 | NP_001311052.1 | |
NM_001324124.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1220 | NP_001311053.1 | |
NM_001324125.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1128 | NP_001311054.1 | |
NM_001324126.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1216 | NP_001311055.1 | |
NM_014608.4 | 4293 | Silent Mutation | CTC,CTT | L,L 1250 | NP_055423.1 | |
XM_011543873.2 | 4293 | Silent Mutation | CTC,CTT | L,L 1383 | XP_011542175.1 | |
XM_011543874.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1383 | XP_011542176.1 | |
XM_011543876.2 | 4293 | Silent Mutation | CTC,CTT | L,L 1282 | XP_011542178.2 | |
XM_017022023.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1417 | XP_016877512.1 | |
XM_017022024.1 | 4293 | Silent Mutation | CTC,CTT | L,L 1383 | XP_016877513.1 |
NIPA2 - non imprinted in Prader-Willi/Angelman syndrome 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |