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CCGACTTCGAGGAAAGGGACGAGTC[C/T]GAAGGTGTGAGTCCGCCCAAACCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614117 MIM: 602438 MIM: 605235 | ||||||||||||||||||||
Literature Links: |
EXOC3L1 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 |
EXOC3L1 - exocyst complex component 3 like 1 | ||||||
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There are no transcripts associated with this gene. |
HSF4 - heat shock transcription factor 4 | ||||||
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There are no transcripts associated with this gene. |
KIAA0895L - KIAA0895 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040715.1 | 807 | Intron | NP_001035805.1 |
NOL3 - nucleolar protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001185057.2 | 807 | Missense Mutation | CCG,CTG | P,L 202 | NP_001171986.1 | |
NM_001276307.1 | 807 | Silent Mutation | TCC,TCT | S,S 205 | NP_001263236.1 | |
NM_001276309.1 | 807 | Silent Mutation | TCC,TCT | S,S 205 | NP_001263238.1 | |
NM_001276311.1 | 807 | Missense Mutation | CCG,CTG | P,L 164 | NP_001263240.1 | |
NM_001276312.1 | 807 | Silent Mutation | TCC,TCT | S,S 205 | NP_001263241.1 | |
NM_001276319.1 | 807 | Silent Mutation | TCC,TCT | S,S 267 | NP_001263248.1 | |
NM_003946.6 | 807 | Silent Mutation | TCC,TCT | S,S 205 | NP_003937.1 | |
XM_005256217.2 | 807 | Missense Mutation | CCG,CTG | P,L 264 | XP_005256274.1 | |
XM_005256219.3 | 807 | Missense Mutation | CCG,CTG | P,L 226 | XP_005256276.1 | |
XM_011523424.2 | 807 | Missense Mutation | CCG,CTG | P,L 202 | XP_011521726.1 | |
XM_017023843.1 | 807 | Silent Mutation | TCC,TCT | S,S 267 | XP_016879332.1 |