Product Details

SNP ID
rs187889757
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:30525894 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCCAAACTCCACGGGCAGCTGGT[C/T]GGGGCTGATGAATTTTGTCAGCTCC
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SEC14L6 PubMed Links

Gene Details

Gene
SEC14L6
Gene Name
SEC14 like lipid binding 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001193336.2 952 Missense Mutation AAC,GAC N235D NP_001180265.2
XM_011530357.2 952 Missense Mutation AAC,GAC N252D XP_011528659.1
XM_011530358.2 952 Missense Mutation AAC,GAC N220D XP_011528660.1
XM_011530360.2 952 Missense Mutation AAC,GAC N189D XP_011528662.1
XM_017028931.1 952 Missense Mutation AAC,GAC N270D XP_016884420.1
XM_017028932.1 952 Missense Mutation AAC,GAC N181D XP_016884421.1
XM_017028933.1 952 Missense Mutation AAC,GAC N238D XP_016884422.1
XM_017028934.1 952 Missense Mutation AAC,GAC N181D XP_016884423.1

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