Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 609807 MIM: 609956 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD300LF PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
|||||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
|||||||||
SAS
|
Japanese
|
JPT (Japanese)
|
|||||||||
AFR
|
Chinese
|
CHB (Han Chinese)
|
|||||||||
EUR
|
|||||||||||
AMR
|
CD300LF - CD300 molecule like family member f | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289082.1 | 863 | Silent Mutation | GCA,GCG | A,A 183 | NP_001276011.1 | |
NM_001289083.1 | 863 | Silent Mutation | GCA,GCG | A,A 233 | NP_001276012.1 | |
NM_001289084.1 | 863 | Missense Mutation | CAA,CGA | Q,R 233 | NP_001276013.1 | |
NM_001289085.1 | 863 | Missense Mutation | CAA,CGA | Q,R 221 | NP_001276014.1 | |
NM_001289086.1 | 863 | Silent Mutation | GCA,GCG | A,A 228 | NP_001276015.1 | |
NM_001289087.1 | 863 | Silent Mutation | GCA,GCG | A,A 210 | NP_001276016.1 | |
NM_139018.4 | 863 | Missense Mutation | CAA,CGA | Q,R 218 | NP_620587.2 | |
XM_017024212.1 | 863 | Missense Mutation | CAA,CGA | Q,R 237 | XP_016879701.1 | |
XM_017024213.1 | 863 | Silent Mutation | GCA,GCG | A,A 255 | XP_016879702.1 | |
XM_017024214.1 | 863 | Silent Mutation | GCA,GCG | A,A 252 | XP_016879703.1 | |
XM_017024215.1 | 863 | Silent Mutation | GCA,GCG | A,A 236 | XP_016879704.1 | |
XM_017024216.1 | 863 | Silent Mutation | GCA,GCG | A,A 229 | XP_016879705.1 | |
XM_017024217.1 | 863 | Silent Mutation | GCA,GCG | A,A 225 | XP_016879706.1 |
RAB37 - RAB37, member RAS oncogene family | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006638.2 | 863 | Intron | NP_001006639.1 | |||
NM_001163989.1 | 863 | Intron | NP_001157461.1 | |||
NM_001163990.1 | 863 | Intron | NP_001157462.1 | |||
NM_175738.4 | 863 | Intron | NP_783865.1 | |||
XM_005257288.4 | 863 | Intron | XP_005257345.1 |
Set Membership: |
HapMap Validated |