Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACAGCGACGCCGCGATTCCGAGGA[C/T]GGAGCCGCGGGAGCCGTGGGTGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 143110 | ||||||||||||||||||||
Literature Links: |
HLA-F 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 |
HLA-F - major histocompatibility complex, class I, F | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098478.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | NP_001091948.1 | |
NM_001098479.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | NP_001091949.1 | |
NM_018950.2 | 227 | Missense Mutation | ACG,ATG | T,M 66 | NP_061823.2 | |
XM_011514564.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | XP_011512866.1 | |
XM_017010810.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | XP_016866299.1 | |
XM_017010811.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | XP_016866300.1 | |
XM_017010812.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | XP_016866301.1 | |
XM_017010813.1 | 227 | Missense Mutation | ACG,ATG | T,M 66 | XP_016866302.1 | |
XM_017010814.1 | 227 | UTR 5 | XP_016866303.1 | |||
XM_017010815.1 | 227 | UTR 5 | XP_016866304.1 |
HLA-F-AS1 - HLA-F antisense RNA 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |