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AATGCTTCCACCAATGGGGGCGCCA[C/T]CACCACTCACACAGGTAATTGTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616288 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FMNL3 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
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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FMNL3 - formin like 3 | ||||||
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There are no transcripts associated with this gene. |
PRPF40B - pre-mRNA processing factor 40 homolog B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031698.2 | 211 | Missense Mutation | CCA,TCA | P,S 72 | NP_001026868.2 | |
NM_012272.2 | 211 | Missense Mutation | CCA,TCA | P,S 44 | NP_036404.1 | |
XM_006719324.3 | 211 | Missense Mutation | ACC,ATC | T,I 143 | XP_006719387.1 | |
XM_006719325.3 | 211 | Missense Mutation | ACC,ATC | T,I 143 | XP_006719388.1 | |
XM_011538135.2 | 211 | Missense Mutation | ACC,ATC | T,I 143 | XP_011536437.1 | |
XM_011538136.2 | 211 | Missense Mutation | ACC,ATC | T,I 143 | XP_011536438.1 | |
XM_011538137.2 | 211 | Missense Mutation | ACC,ATC | T,I 116 | XP_011536439.1 | |
XM_011538138.2 | 211 | Missense Mutation | ACC,ATC | T,I 143 | XP_011536440.1 | |
XM_011538139.2 | 211 | Missense Mutation | CCA,TCA | P,S 72 | XP_011536441.1 | |
XM_011538140.2 | 211 | Missense Mutation | CCA,TCA | P,S 72 | XP_011536442.1 | |
XM_011538141.1 | 211 | Missense Mutation | CCA,TCA | P,S 50 | XP_011536443.1 | |
XM_011538143.2 | 211 | Missense Mutation | CCA,TCA | P,S 45 | XP_011536445.1 | |
XM_011538144.2 | 211 | Missense Mutation | CCA,TCA | P,S 50 | XP_011536446.1 | |
XM_017019135.1 | 211 | Missense Mutation | CCA,TCA | P,S 44 | XP_016874624.1 | |
XM_017019136.1 | 211 | Missense Mutation | CCA,TCA | P,S 50 | XP_016874625.1 | |
XM_017019137.1 | 211 | Missense Mutation | CCA,TCA | P,S 50 | XP_016874626.1 | |
XM_017019138.1 | 211 | Missense Mutation | ACC,ATC | T,I 143 | XP_016874627.1 | |
XM_017019139.1 | 211 | Intron | XP_016874628.1 |