Product Details
- SNP ID
-
rs201092922
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
13
- Location
-
Chr.1:152302945 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATTCACCATAATCATAATCTGCAC[C/T]ACCATAGCTGCCATGTCTCCAAACT
- Phenotype
-
MIM: 135940
- Polymorphism
- C/T, 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 |
11977 |
Missense Mutation |
AGT,GGT |
S3981G |
NP_002007.1 |
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