Product Details
- SNP ID
-
rs2234929
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
9
- Location
-
Chr.1:171635976 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGTGACCATGTTCAAGTTGTCCCA[A/G]GCAAAGAGCTTCTTCTCCAGGGGGT
- Phenotype
-
MIM: 601652
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MYOC
PubMed Links
Gene Details
- Gene
- MYOC
- Gene Name
- myocilin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_000261.1 |
1486 |
Silent Mutation |
|
|
NP_000252.1 |
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