Product Details

SNP ID

rs61742115

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:30531970 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCAGCCCTTCGAGACCAAAAATA[C/G]CTATGATTTTCTCCACCCTCTTCCC

Phenotype

Polymorphism

C/G, Transversion 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	701	Missense Mutation	GCT,GGT	A151G	NP_001180265.2
XM_011530357.2	701	Missense Mutation	GCT,GGT	A168G	XP_011528659.1
XM_011530358.2	701	Intron			XP_011528660.1
XM_011530360.2	701	Missense Mutation	GCT,GGT	A105G	XP_011528662.1
XM_017028931.1	701	Missense Mutation	GCT,GGT	A186G	XP_016884420.1
XM_017028932.1	701	Missense Mutation	GCT,GGT	A97G	XP_016884421.1
XM_017028933.1	701	Missense Mutation	GCT,GGT	A154G	XP_016884422.1
XM_017028934.1	701	Missense Mutation	GCT,GGT	A97G	XP_016884423.1

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