Product Details

SNP ID

rs150078715

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:92463846 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCTAATGCCTGAATGTGTTTTTG[C/G]AAGGCCTCTTCTGTCATGTCCTCTA

Phenotype

MIM: 146680

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

IDE PubMed Links

Gene Details

Gene

IDE

Gene Name

insulin degrading enzyme

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001165946.1	1306	Missense Mutation	TTC,TTG	F327L	NP_001159418.1
NM_001322793.1	1306	Missense Mutation	TTC,TTG	F882L	NP_001309722.1
NM_001322794.1	1306	Missense Mutation	TTC,TTG	F843L	NP_001309723.1
NM_001322795.1	1306	Missense Mutation	TTC,TTG	F841L	NP_001309724.1
NM_001322796.1	1306	Missense Mutation	TTC,TTG	F841L	NP_001309725.1
NM_001322797.1	1306	Missense Mutation	TTC,TTG	F327L	NP_001309726.1
NM_004969.3	1306	Missense Mutation	TTC,TTG	F882L	NP_004960.2
XM_017016187.1	1306	Missense Mutation	TTC,TTG	F841L	XP_016871676.1
XM_017016188.1	1306	Missense Mutation	TTC,TTG	F841L	XP_016871677.1
XM_017016189.1	1306	Missense Mutation	TTC,TTG	F841L	XP_016871678.1
XM_017016190.1	1306	Missense Mutation	TTC,TTG	F841L	XP_016871679.1

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