Product Details
- SNP ID
-
rs3903257
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:219418530 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGCCGCACCTTCGGCGGGGCCCCGG[G/T]CTTCCCACTCGGCTCCCCGCTGAGT
- Phenotype
-
MIM: 125660
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
DES
PubMed Links
Gene Details
- Gene
- DES
- Gene Name
- desmin
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001927.3 |
154 |
Missense Mutation |
GGC,GTC |
G23V |
NP_001918.3 |
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