Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCTCTGTGAGTTACCACACCCAG[G/C]ATTCCTCCTGATCCCAGAGAAATCG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 306250 MIM: 425000 | |||||||||||||||||||||||
Literature Links: |
CSF2RA PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
CSF2RA - colony stimulating factor 2 receptor alpha subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161529.1 | 211 | Missense Mutation | GCA,GGA | A,G 17 | NP_001155001.1 | |
NM_001161530.1 | 211 | Intron | NP_001155002.1 | |||
NM_001161531.1 | 211 | Missense Mutation | GCA,GGA | A,G 17 | NP_001155003.1 | |
NM_001161532.1 | 211 | Intron | NP_001155004.1 | |||
NM_006140.4 | 211 | Missense Mutation | GCA,GGA | A,G 17 | NP_006131.2 | |
NM_172245.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | NP_758448.1 | |
NM_172246.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | NP_758449.1 | |
NM_172247.2 | 211 | Intron | NP_758450.1 | |||
NM_172249.2 | 211 | Intron | NP_758452.1 | |||
XM_011546165.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544467.1 | |
XM_011546166.1 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544468.1 | |
XM_011546167.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544469.1 | |
XM_011546168.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544470.1 | |
XM_011546169.1 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544471.1 | |
XM_011546170.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544472.1 | |
XM_011546173.1 | 211 | Intron | XP_011544475.1 | |||
XM_011546174.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544476.1 | |
XM_011546175.2 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_011544477.1 | |
XM_017029287.1 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_016884776.1 | |
XM_017029288.1 | 211 | Missense Mutation | GCA,GGA | A,G 17 | XP_016884777.1 |