Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
30 submissions
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Phenotype: |
MIM: 138971 MIM: 611979 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CSF3R 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)
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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 | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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CSF3R - colony stimulating factor 3 receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000760.3 | 2238 | Intron | NP_000751.1 | |||
NM_156039.3 | 2238 | Missense Mutation | CGT,TGT | R,C 698 | NP_724781.1 | |
NM_172313.2 | 2238 | Intron | NP_758519.1 | |||
XM_005270493.1 | 2238 | Intron | XP_005270550.1 | |||
XM_011540748.2 | 2238 | Missense Mutation | CGT,TGT | R,C 698 | XP_011539050.1 | |
XM_011540749.1 | 2238 | Missense Mutation | CGT,TGT | R,C 697 | XP_011539051.1 | |
XM_011540750.1 | 2238 | Missense Mutation | CGT,TGT | R,C 474 | XP_011539052.1 | |
XM_017000370.1 | 2238 | Missense Mutation | CGT,TGT | R,C 698 | XP_016855859.1 |
MRPS15 - mitochondrial ribosomal protein S15 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |