Product Details
- SNP ID
-
rs150002541
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
5
- Location
-
Chr.1:152409811 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTCTCCCTGCCCTTCTGTCACACAG[C/G]GCCTTGGGTGAGTGCTGCTCCACTC
- Phenotype
-
MIM: 611312
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
CRNN
PubMed Links
Gene Details
- Gene
- CRNN
- Gene Name
- cornulin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_016190.2 |
1345 |
Missense Mutation |
CCC,CGC |
P424R |
NP_057274.1 |
View Full Product Details