Product Details

SNP ID
rs4930556
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64610254 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCCAGGGCTCCTGGCCCTCCAAAG[C/G]CTCAGTCACAGTGAAAAACTTTGAG
Phenotype
MIM: 600566 MIM: 607096
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
NRXN2 PubMed Links

Gene Details

Gene
NRXN2
Gene Name
neurexin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015080.3 Intron NP_055895.1
NM_138732.2 Intron NP_620060.1
NM_138734.2 Intron NP_620063.1
XM_005274400.3 Intron XP_005274457.1
XM_005274401.3 Intron XP_005274458.1
XM_005274402.3 Intron XP_005274459.1
XM_011545370.1 Intron XP_011543672.1
XM_011545371.1 Intron XP_011543673.1
XM_011545373.1 Intron XP_011543675.1
XM_011545375.1 Intron XP_011543677.1
XM_011545385.1 Intron XP_011543687.1
XM_017018563.1 Intron XP_016874052.1
XM_017018564.1 Intron XP_016874053.1
XM_017018565.1 Intron XP_016874054.1
XM_017018566.1 Intron XP_016874055.1
XM_017018567.1 Intron XP_016874056.1
XM_017018568.1 Intron XP_016874057.1
XM_017018569.1 Intron XP_016874058.1
XM_017018570.1 Intron XP_016874059.1
XM_017018571.1 Intron XP_016874060.1
XM_017018572.1 Intron XP_016874061.1
XM_017018573.1 Intron XP_016874062.1
XM_017018574.1 Intron XP_016874063.1
XM_017018575.1 Intron XP_016874064.1
XM_017018576.1 Intron XP_016874065.1
XM_017018577.1 Intron XP_016874066.1
XM_017018578.1 Intron XP_016874067.1
Gene
SLC22A12
Gene Name
solute carrier family 22 member 12
There are no transcripts associated with this gene.

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