Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGGAACGGGAGCGGGCCCGGCTTC[A/G]GGAGCGACGCCAACAACGCAAGAAT
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 |
---|---|---|
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 |
FMNL3 - formin like 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_175736.4 | 1406 | Intron | NP_783863.4 | |||
NM_198900.2 | 1406 | Intron | NP_944489.2 | |||
XM_005269218.2 | 1406 | UTR 3 | XP_005269275.1 | |||
XM_011538968.2 | 1406 | UTR 3 | XP_011537270.1 | |||
XM_011538969.2 | 1406 | UTR 3 | XP_011537271.1 | |||
XM_011538970.2 | 1406 | UTR 3 | XP_011537272.1 | |||
XM_011538971.2 | 1406 | UTR 3 | XP_011537273.1 | |||
XM_011538972.2 | 1406 | UTR 3 | XP_011537274.1 | |||
XM_011538973.2 | 1406 | UTR 3 | XP_011537275.2 | |||
XM_011538974.2 | 1406 | UTR 3 | XP_011537276.1 |
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 | 1406 | Missense Mutation | CAG,CGG | Q,R 507 | NP_001026868.2 | |
NM_012272.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 479 | NP_036404.1 | |
XM_006719324.3 | 1406 | Missense Mutation | CAG,CGG | Q,R 569 | XP_006719387.1 | |
XM_006719325.3 | 1406 | Missense Mutation | CAG,CGG | Q,R 569 | XP_006719388.1 | |
XM_011538135.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 569 | XP_011536437.1 | |
XM_011538136.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 569 | XP_011536438.1 | |
XM_011538137.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 542 | XP_011536439.1 | |
XM_011538138.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 532 | XP_011536440.1 | |
XM_011538139.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 507 | XP_011536441.1 | |
XM_011538140.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 507 | XP_011536442.1 | |
XM_011538141.1 | 1406 | Missense Mutation | CAG,CGG | Q,R 485 | XP_011536443.1 | |
XM_011538143.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 480 | XP_011536445.1 | |
XM_011538144.2 | 1406 | Missense Mutation | CAG,CGG | Q,R 448 | XP_011536446.1 | |
XM_017019135.1 | 1406 | Missense Mutation | CAG,CGG | Q,R 479 | XP_016874624.1 | |
XM_017019136.1 | 1406 | Missense Mutation | CAG,CGG | Q,R 448 | XP_016874625.1 | |
XM_017019137.1 | 1406 | Missense Mutation | CAG,CGG | Q,R 448 | XP_016874626.1 | |
XM_017019138.1 | 1406 | Missense Mutation | CAG,CGG | Q,R 569 | XP_016874627.1 | |
XM_017019139.1 | 1406 | Missense Mutation | CAG,CGG | Q,R 184 | XP_016874628.1 |