Product Details
- SNP ID
-
rs149386596
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:64607350 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CACCTGGTAGGAGCCCTCATCACGA[C/T]TGCGGTACTTATACATGGCGTAGAG
- Phenotype
-
MIM: 600566
MIM: 607096
- Polymorphism
- C/T, Transition 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 |
3345 |
Missense Mutation |
AAT,AGT |
N1662S |
NP_055895.1 |
NM_138732.2 |
3345 |
Missense Mutation |
AAT,AGT |
N1592S |
NP_620060.1 |
NM_138734.2 |
3345 |
Missense Mutation |
AAT,AGT |
N616S |
NP_620063.1 |
XM_005274400.3 |
3345 |
Missense Mutation |
AAT,AGT |
N1655S |
XP_005274457.1 |
XM_005274401.3 |
3345 |
Missense Mutation |
AAT,AGT |
N1461S |
XP_005274458.1 |
XM_005274402.3 |
3345 |
Missense Mutation |
AAT,AGT |
N1453S |
XP_005274459.1 |
XM_011545370.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1665S |
XP_011543672.1 |
XM_011545371.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1664S |
XP_011543673.1 |
XM_011545373.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1658S |
XP_011543675.1 |
XM_011545375.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1650S |
XP_011543677.1 |
XM_011545385.1 |
3345 |
Missense Mutation |
AAT,AGT |
N927S |
XP_011543687.1 |
XM_017018563.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1655S |
XP_016874052.1 |
XM_017018564.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1654S |
XP_016874053.1 |
XM_017018565.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1653S |
XP_016874054.1 |
XM_017018566.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1641S |
XP_016874055.1 |
XM_017018567.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1635S |
XP_016874056.1 |
XM_017018568.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1632S |
XP_016874057.1 |
XM_017018569.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1631S |
XP_016874058.1 |
XM_017018570.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1471S |
XP_016874059.1 |
XM_017018571.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1468S |
XP_016874060.1 |
XM_017018572.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1430S |
XP_016874061.1 |
XM_017018573.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1429S |
XP_016874062.1 |
XM_017018574.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1420S |
XP_016874063.1 |
XM_017018575.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1419S |
XP_016874064.1 |
XM_017018576.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1246S |
XP_016874065.1 |
XM_017018577.1 |
3345 |
Missense Mutation |
AAT,AGT |
N924S |
XP_016874066.1 |
XM_017018578.1 |
3345 |
Missense Mutation |
AAT,AGT |
N1438S |
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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