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Search Thermo Fisher Scientific
TGATGGCCAGAACCACCTTGGGGCT[A/G]GACATGGCTGACACCTTCACCAGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138970 MIM: 607000 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CSF3 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) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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CSF3 - colony stimulating factor 3 | ||||||
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There are no transcripts associated with this gene. |
MED24 - mediator complex subunit 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079518.1 | 3069 | Silent Mutation | TCC,TCT | S,S 949 | NP_001072986.1 | |
NM_001267797.1 | 3069 | Silent Mutation | TCC,TCT | S,S 949 | NP_001254726.1 | |
NM_014815.3 | 3069 | Silent Mutation | TCC,TCT | S,S 962 | NP_055630.2 | |
XM_005257874.2 | 3069 | Silent Mutation | TCC,TCT | S,S 987 | XP_005257931.1 | |
XM_006722204.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1042 | XP_006722267.1 | |
XM_006722206.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1017 | XP_006722269.1 | |
XM_006722207.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1017 | XP_006722270.1 | |
XM_011525529.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1061 | XP_011523831.1 | |
XM_011525530.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1024 | XP_011523832.1 | |
XM_011525531.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1005 | XP_011523833.1 | |
XM_011525532.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1036 | XP_011523834.1 | |
XM_011525533.2 | 3069 | Silent Mutation | TCC,TCT | S,S 1036 | XP_011523835.1 | |
XM_011525534.2 | 3069 | Silent Mutation | TCC,TCT | S,S 993 | XP_011523836.1 | |
XM_011525535.2 | 3069 | Silent Mutation | TCC,TCT | S,S 992 | XP_011523837.1 | |
XM_011525536.2 | 3069 | Silent Mutation | TCC,TCT | S,S 981 | XP_011523838.1 | |
XM_011525538.2 | 3069 | Silent Mutation | TCC,TCT | S,S 920 | XP_011523840.1 | |
XM_017025458.1 | 3069 | Silent Mutation | TCC,TCT | S,S 1024 | XP_016880947.1 | |
XM_017025459.1 | 3069 | Silent Mutation | TCC,TCT | S,S 1005 | XP_016880948.1 | |
XM_017025460.1 | 3069 | Silent Mutation | TCC,TCT | S,S 981 | XP_016880949.1 | |
XM_017025461.1 | 3069 | Silent Mutation | TCC,TCT | S,S 1006 | XP_016880950.1 | |
XM_017025462.1 | 3069 | Silent Mutation | TCC,TCT | S,S 980 | XP_016880951.1 | |
XM_017025463.1 | 3069 | Silent Mutation | TCC,TCT | S,S 980 | XP_016880952.1 | |
XM_017025464.1 | 3069 | Silent Mutation | TCC,TCT | S,S 974 | XP_016880953.1 | |
XM_017025465.1 | 3069 | Silent Mutation | TCC,TCT | S,S 999 | XP_016880954.1 | |
XM_017025466.1 | 3069 | Silent Mutation | TCC,TCT | S,S 962 | XP_016880955.1 | |
XM_017025467.1 | 3069 | Silent Mutation | TCC,TCT | S,S 961 | XP_016880956.1 | |
XM_017025468.1 | 3069 | Silent Mutation | TCC,TCT | S,S 961 | XP_016880957.1 | |
XM_017025469.1 | 3069 | Silent Mutation | TCC,TCT | S,S 908 | XP_016880958.1 | |
XM_017025470.1 | 3069 | Silent Mutation | TCC,TCT | S,S 865 | XP_016880959.1 | |
XM_017025471.1 | 3069 | Intron | XP_016880960.1 |
MIR6884 - microRNA 6884 | ||||||
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There are no transcripts associated with this gene. |
SNORD124 - small nucleolar RNA, C/D box 124 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |