Product Details
- SNP ID
-
rs2233069
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:23644697 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCTCTCATCCAAGGGAGACAAGG[A/G]CTGTGCCTCCACCTTGGAATTATCC
- Phenotype
-
MIM: 605283
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MAGEL2
PubMed Links
Gene Details
- Gene
- MAGEL2
- Gene Name
- MAGE family member L2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_019066.4 |
3150 |
Missense Mutation |
CCC,TCC |
P1016S |
NP_061939.3 |
View Full Product Details