Product Details

SNP ID
rs7302676
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:44508481 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATTTCTTTTCAGAGTGTACTGTACA[C/T]AACATGTTATAGCTTCTTTGCTTTA
Phenotype
MIM: 602320
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NELL2 PubMed Links

Gene Details

Gene
NELL2
Gene Name
neural EGFL like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145107.1 3179 UTR 3 NP_001138579.1
NM_001145108.1 3179 UTR 3 NP_001138580.1
NM_001145109.1 3179 UTR 3 NP_001138581.1
NM_001145110.1 3179 UTR 3 NP_001138582.1
NM_006159.2 3179 UTR 3 NP_006150.1
XM_005268905.3 3179 UTR 3 XP_005268962.1
XM_011538396.1 3179 UTR 3 XP_011536698.1
XM_017019341.1 3179 UTR 3 XP_016874830.1
XM_017019342.1 3179 UTR 3 XP_016874831.1
XM_017019343.1 3179 UTR 3 XP_016874832.1
XM_017019344.1 3179 UTR 3 XP_016874833.1

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