Product Details
- SNP ID
-
rs202141423
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:46859510 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGCACGTGGCGAAGCTCAGCACCC[A/G]TGACAGTGCCATTGCCCTCCTTGTC
- Phenotype
-
MIM: 160790
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MYL3
PubMed Links
Gene Details
- Gene
- MYL3
- Gene Name
- myosin light chain 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_000258.2 |
539 |
Missense Mutation |
ACG,ATG |
T149M |
NP_000249.1 |
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