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Search Thermo Fisher Scientific
TCCTCAGCACCCAAGGTCAGAGATG[C/T]ATAGGAAATGTCCTCCTTCGGCAAG
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 |
---|---|---|
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 |
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 | 958 | UTR 3 | NP_001276011.1 | |||
NM_001289083.1 | 958 | UTR 3 | NP_001276012.1 | |||
NM_001289084.1 | 958 | Missense Mutation | ACA,GCA | T,A 265 | NP_001276013.1 | |
NM_001289085.1 | 958 | Missense Mutation | ACA,GCA | T,A 253 | NP_001276014.1 | |
NM_001289086.1 | 958 | UTR 3 | NP_001276015.1 | |||
NM_001289087.1 | 958 | UTR 3 | NP_001276016.1 | |||
NM_139018.4 | 958 | Missense Mutation | ACA,GCA | T,A 250 | NP_620587.2 | |
XM_017024212.1 | 958 | Missense Mutation | ACA,GCA | T,A 269 | XP_016879701.1 | |
XM_017024213.1 | 958 | UTR 3 | XP_016879702.1 | |||
XM_017024214.1 | 958 | UTR 3 | XP_016879703.1 | |||
XM_017024215.1 | 958 | UTR 3 | XP_016879704.1 | |||
XM_017024216.1 | 958 | UTR 3 | XP_016879705.1 | |||
XM_017024217.1 | 958 | UTR 3 | 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 | 958 | Intron | NP_001006639.1 | |||
NM_001163989.1 | 958 | Intron | NP_001157461.1 | |||
NM_001163990.1 | 958 | Intron | NP_001157462.1 | |||
NM_175738.4 | 958 | Intron | NP_783865.1 | |||
XM_005257288.4 | 958 | Intron | XP_005257345.1 |