Product Details
- SNP ID
-
rs12947361
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:41567397 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCACTTCCTCCACCATGGCTGCCT[C/G]CACTTCCTCCCCTGGACCCACTTCC
- Phenotype
-
MIM: 607606
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
KRT9
PubMed Links
Gene Details
- Gene
- KRT9
- Gene Name
- keratin 9
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_000226.3 |
1814 |
Missense Mutation |
GCA,GGA |
A583G |
NP_000217.2 |
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