Product Details

SNP ID

rs150895887

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:18078506 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACCTTCTGGAGGAGGCGGCCGAC[C/T]TCCTGGTGGTGCACCTGGACTTCCG

Phenotype

MIM: 608666

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PEX26 PubMed Links

Gene Details

Gene

PEX26

Gene Name

peroxisomal biogenesis factor 26

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127649.2	339	Missense Mutation	CTC,TTC	L44F	NP_001121121.1
NM_001199319.1	339	Missense Mutation	CTC,TTC	L44F	NP_001186248.1
NM_017929.5	339	Missense Mutation	CTC,TTC	L44F	NP_060399.1

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