Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCCCAAACTCCACGGGCAGCTGGT[C/T]GGGGCTGATGAATTTTGTCAGCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SEC14L6 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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SEC14L6 - SEC14 like lipid binding 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193336.2 | 952 | Missense Mutation | AAC,GAC | N,D 235 | NP_001180265.2 | |
XM_011530357.2 | 952 | Missense Mutation | AAC,GAC | N,D 252 | XP_011528659.1 | |
XM_011530358.2 | 952 | Missense Mutation | AAC,GAC | N,D 220 | XP_011528660.1 | |
XM_011530360.2 | 952 | Missense Mutation | AAC,GAC | N,D 189 | XP_011528662.1 | |
XM_017028931.1 | 952 | Missense Mutation | AAC,GAC | N,D 270 | XP_016884420.1 | |
XM_017028932.1 | 952 | Missense Mutation | AAC,GAC | N,D 181 | XP_016884421.1 | |
XM_017028933.1 | 952 | Missense Mutation | AAC,GAC | N,D 238 | XP_016884422.1 | |
XM_017028934.1 | 952 | Missense Mutation | AAC,GAC | N,D 181 | XP_016884423.1 |