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GTGGTAGCCTTTTGCGGGGAGGTTC[C/T]GGCCAGCTGCAGGGTCAGGTCTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609807 MIM: 609956 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD300LF PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CD300LF - CD300 molecule like family member f | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289082.1 | 850 | Missense Mutation | CAG,CGG | Q,R 179 | NP_001276011.1 | |
NM_001289083.1 | 850 | Missense Mutation | CAG,CGG | Q,R 229 | NP_001276012.1 | |
NM_001289084.1 | 850 | Missense Mutation | AGA,GGA | R,G 229 | NP_001276013.1 | |
NM_001289085.1 | 850 | Missense Mutation | AGA,GGA | R,G 217 | NP_001276014.1 | |
NM_001289086.1 | 850 | Missense Mutation | CAG,CGG | Q,R 224 | NP_001276015.1 | |
NM_001289087.1 | 850 | Missense Mutation | CAG,CGG | Q,R 206 | NP_001276016.1 | |
NM_139018.4 | 850 | Missense Mutation | AGA,GGA | R,G 214 | NP_620587.2 | |
XM_017024212.1 | 850 | Missense Mutation | AGA,GGA | R,G 233 | XP_016879701.1 | |
XM_017024213.1 | 850 | Missense Mutation | CAG,CGG | Q,R 251 | XP_016879702.1 | |
XM_017024214.1 | 850 | Missense Mutation | CAG,CGG | Q,R 248 | XP_016879703.1 | |
XM_017024215.1 | 850 | Missense Mutation | CAG,CGG | Q,R 232 | XP_016879704.1 | |
XM_017024216.1 | 850 | Missense Mutation | CAG,CGG | Q,R 225 | XP_016879705.1 | |
XM_017024217.1 | 850 | Missense Mutation | CAG,CGG | Q,R 221 | XP_016879706.1 |
RAB37 - RAB37, member RAS oncogene family | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006638.2 | 850 | Intron | NP_001006639.1 | |||
NM_001163989.1 | 850 | Intron | NP_001157461.1 | |||
NM_001163990.1 | 850 | Intron | NP_001157462.1 | |||
NM_175738.4 | 850 | Intron | NP_783865.1 | |||
XM_005257288.4 | 850 | Intron | XP_005257345.1 |