Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTAATCAGAAGAGACTGGCAGGGGG[A/G]GAAACAAGATTGCTTTCTGGCCATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131220 | ||||||||||||||||||||
Literature Links: |
FGF1 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 |
FGF1 - fibroblast growth factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000800.4 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_000791.1 | |
NM_001144892.2 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001138364.1 | |
NM_001144934.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001138406.1 | |
NM_001144935.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001138407.1 | |
NM_001257205.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001244134.1 | |
NM_001257206.1 | 370 | Missense Mutation | CCC,CTC | P,L 147 | NP_001244135.1 | |
NM_001257207.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001244136.1 | |
NM_001257208.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001244137.1 | |
NM_001257209.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001244138.1 | |
NM_001257210.1 | 370 | Missense Mutation | CCC,CTC | P,L 148 | NP_001244139.1 | |
NM_001257211.1 | 370 | Missense Mutation | CCC,CTC | P,L 147 | NP_001244140.1 | |
NM_001257212.1 | 370 | Missense Mutation | CCC,CTC | P,L 147 | NP_001244141.1 | |
NM_033136.3 | 370 | UTR 3 | NP_149127.1 | |||
NM_033137.2 | 370 | UTR 3 | NP_149128.1 | |||
XM_005268390.4 | 370 | Missense Mutation | CCC,CTC | P,L 147 | XP_005268447.1 | |
XM_011537607.2 | 370 | Missense Mutation | CCC,CTC | P,L 147 | XP_011535909.1 |