Product Details
- SNP ID
-
rs201971901
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
4
- Location
-
Chr.1:152909834 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACACACACTGCCAGTGACCCTCTCC[C/T]CTGCCCTCAGTCAGGAGCTCCTCAA
- Phenotype
-
MIM: 147360
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
IVL
PubMed Links
Gene Details
- Gene
- IVL
- Gene Name
- involucrin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005547.2 |
83 |
Missense Mutation |
CCT,TCT |
P13S |
NP_005538.2 |
View Full Product Details