Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGAAGCGGGCAGTGAGCCTGCCCC[C/T]GAACAGGAGAGCACCGAAGCTACAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607686 MIM: 609732 | ||||||||||||||||||||
Literature Links: |
FIP1L1 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 |
FIP1L1 - factor interacting with PAPOLA and CPSF1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134937.1 | 4185 | Silent Mutation | CCC,CCT | P,P 577 | NP_001128409.1 | |
NM_001134938.1 | 4185 | Silent Mutation | CCC,CCT | P,P 509 | NP_001128410.1 | |
NM_030917.3 | 4185 | Silent Mutation | CCC,CCT | P,P 583 | NP_112179.2 | |
XM_005265769.4 | 4185 | Silent Mutation | CCC,CCT | P,P 592 | XP_005265826.1 | |
XM_005265773.4 | 4185 | Silent Mutation | CCC,CCT | P,P 569 | XP_005265830.1 | |
XM_005265774.4 | 4185 | Silent Mutation | CCC,CCT | P,P 560 | XP_005265831.1 | |
XM_005265778.4 | 4185 | Missense Mutation | CCG,CTG | P,L 521 | XP_005265835.1 | |
XM_005265779.4 | 4185 | Missense Mutation | CCG,CTG | P,L 512 | XP_005265836.1 | |
XM_005265781.4 | 4185 | Silent Mutation | CCC,CCT | P,P 533 | XP_005265838.1 | |
XM_005265782.4 | 4185 | Silent Mutation | CCC,CCT | P,P 524 | XP_005265839.1 | |
XM_017008662.1 | 4185 | Silent Mutation | CCC,CCT | P,P 568 | XP_016864151.1 | |
XM_017008663.1 | 4185 | Silent Mutation | CCC,CCT | P,P 556 | XP_016864152.1 | |
XM_017008664.1 | 4185 | Silent Mutation | CCC,CCT | P,P 554 | XP_016864153.1 | |
XM_017008665.1 | 4185 | Silent Mutation | CCC,CCT | P,P 547 | XP_016864154.1 | |
XM_017008666.1 | 4185 | Silent Mutation | CCC,CCT | P,P 545 | XP_016864155.1 | |
XM_017008667.1 | 4185 | Silent Mutation | CCC,CCT | P,P 541 | XP_016864156.1 | |
XM_017008668.1 | 4185 | Silent Mutation | CCC,CCT | P,P 532 | XP_016864157.1 | |
XM_017008669.1 | 4185 | Silent Mutation | CCC,CCT | P,P 518 | XP_016864158.1 | |
XM_017008670.1 | 4185 | Missense Mutation | CCG,CTG | P,L 489 | XP_016864159.1 | |
XM_017008671.1 | 4185 | Missense Mutation | CCG,CTG | P,L 462 | XP_016864160.1 |
LNX1 - ligand of numb-protein X 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001126328.2 | 4185 | Intron | NP_001119800.1 | |||
NM_032622.2 | 4185 | Intron | NP_116011.2 | |||
XM_005265785.4 | 4185 | UTR 3 | XP_005265842.1 | |||
XM_017008776.1 | 4185 | UTR 3 | XP_016864265.1 |