Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGGTAGGGTGAGGAAGGCTATTTG[C/G]GGGGGCCCGGGGGGATCTGCAGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 605536 MIM: 615572 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAB11FIP5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
RAB11FIP5 - RAB11 family interacting protein 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015470.2 | 4150 | Missense Mutation | CCC,CGC | P,R 652 | NP_056285.1 | |
XM_005264251.3 | 4150 | Missense Mutation | CCC,CGC | P,R 1217 | XP_005264308.1 | |
XM_005264252.3 | 4150 | Missense Mutation | CCC,CGC | P,R 1323 | XP_005264309.1 | |
XM_005264253.4 | 4150 | Intron | XP_005264310.1 | |||
XM_006711985.3 | 4150 | Missense Mutation | CCC,CGC | P,R 1248 | XP_006712048.1 | |
XM_011532753.2 | 4150 | Missense Mutation | CCC,CGC | P,R 1117 | XP_011531055.1 | |
XM_011532754.2 | 4150 | Intron | XP_011531056.1 | |||
XM_011532755.2 | 4150 | Intron | XP_011531057.1 | |||
XM_011532756.2 | 4150 | Intron | XP_011531058.1 | |||
XM_017003788.1 | 4150 | Missense Mutation | CCC,CGC | P,R 1072 | XP_016859277.1 |
SFXN5 - sideroflexin 5 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |