Product Details

SNP ID
rs11246286
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:715420 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCCCTCTTTTGTTCTGGTTTTTGA[A/G]AATTTGTGTTTTCTCTAGTATTTTT
Phenotype
MIM: 614988
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EPS8L2 PubMed Links

Gene Details

Gene
EPS8L2
Gene Name
EPS8 like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022772.3 Intron NP_073609.2
XM_017018130.1 Intron XP_016873619.1
XM_017018131.1 Intron XP_016873620.1
XM_017018132.1 Intron XP_016873621.1

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