Product Details
- SNP ID
-
rs193143179
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:64607757 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGGAGCGGGTTTGCGGGGTGACAG[G/T]AGGGTGGTGCGGTCCGTGACCAGGG
- Phenotype
-
MIM: 600566
MIM: 607096
- Polymorphism
- G/T, 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 |
2938 |
Silent Mutation |
CTA,CTC |
L1526L |
NP_055895.1 |
| NM_138732.2 |
2938 |
Silent Mutation |
CTA,CTC |
L1456L |
NP_620060.1 |
| NM_138734.2 |
2938 |
Silent Mutation |
CTA,CTC |
L480L |
NP_620063.1 |
| XM_005274400.3 |
2938 |
Silent Mutation |
CTA,CTC |
L1519L |
XP_005274457.1 |
| XM_005274401.3 |
2938 |
Intron |
|
|
XP_005274458.1 |
| XM_005274402.3 |
2938 |
Intron |
|
|
XP_005274459.1 |
| XM_011545370.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1529L |
XP_011543672.1 |
| XM_011545371.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1528L |
XP_011543673.1 |
| XM_011545373.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1522L |
XP_011543675.1 |
| XM_011545375.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1514L |
XP_011543677.1 |
| XM_011545385.1 |
2938 |
Silent Mutation |
CTA,CTC |
L791L |
XP_011543687.1 |
| XM_017018563.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1519L |
XP_016874052.1 |
| XM_017018564.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1518L |
XP_016874053.1 |
| XM_017018565.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1517L |
XP_016874054.1 |
| XM_017018566.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1505L |
XP_016874055.1 |
| XM_017018567.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1499L |
XP_016874056.1 |
| XM_017018568.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1496L |
XP_016874057.1 |
| XM_017018569.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1495L |
XP_016874058.1 |
| XM_017018570.1 |
2938 |
Intron |
|
|
XP_016874059.1 |
| XM_017018571.1 |
2938 |
Intron |
|
|
XP_016874060.1 |
| XM_017018572.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1294L |
XP_016874061.1 |
| XM_017018573.1 |
2938 |
Intron |
|
|
XP_016874062.1 |
| XM_017018574.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1284L |
XP_016874063.1 |
| XM_017018575.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1283L |
XP_016874064.1 |
| XM_017018576.1 |
2938 |
Silent Mutation |
CTA,CTC |
L1110L |
XP_016874065.1 |
| XM_017018577.1 |
2938 |
Silent Mutation |
CTA,CTC |
L788L |
XP_016874066.1 |
| XM_017018578.1 |
2938 |
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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