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- SNP ID:
- rs2287015
- Gene
-
FLVCR2LOC102724153 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.14: 75579019 - 75579019 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CAGGAAGAGAGCGATGACACCCCTG[C/T]GCCGGAGTCCGCACTCCAAGCGGAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610865
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Literature Links: |
FLVCR2 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| FLVCR2 - feline leukemia virus subgroup C cellular receptor family member 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001195283.1 | 423 | Intron | NP_001182212.1 | |||
| NM_017791.2 | 423 | Missense Mutation | GCG,GTG | A,V 16 | NP_060261.2 | |
| LOC102724153 - uncharacterized LOC102724153 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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