Product Details

SNP ID
rs150330138
Assay Type
Functionally tested
NCBI dbSNP Submissions
10
Location
Chr.1:152302800 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCTGGGTCCTTATTAATATACGTT[A/G]CATAATACCTTGGATGATCTTTACC
Phenotype
MIM: 135940
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FLG PubMed Links

Gene Details

Gene
FLG
Gene Name
filaggrin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002016.1 12122 Missense Mutation GCA,GTA A4029V NP_002007.1

View Full Product Details