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- SNP ID:
- rs200024020
- Gene
-
NRXN2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 64651517 - 64651517 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TCCATGTAGGGCTGGCCATTGAACA[C/T]GAGCCCACTCAGATGCCCGATGAAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600566
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Literature Links: |
NRXN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| NRXN2 - neurexin 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_015080.3 | 1016 | Missense Mutation | ATG,GTG | M,V 886 | NP_055895.1 | |
| NM_138732.2 | 1016 | Missense Mutation | ATG,GTG | M,V 846 | NP_620060.1 | |
| NM_138734.2 | 1016 | Intron | NP_620063.1 | |||
| XM_005274400.3 | 1016 | Missense Mutation | ATG,GTG | M,V 879 | XP_005274457.1 | |
| XM_005274401.3 | 1016 | Missense Mutation | ATG,GTG | M,V 879 | XP_005274458.1 | |
| XM_005274402.3 | 1016 | Missense Mutation | ATG,GTG | M,V 871 | XP_005274459.1 | |
| XM_011545370.1 | 1016 | Missense Mutation | ATG,GTG | M,V 889 | XP_011543672.1 | |
| XM_011545371.1 | 1016 | Missense Mutation | ATG,GTG | M,V 888 | XP_011543673.1 | |
| XM_011545373.1 | 1016 | Missense Mutation | ATG,GTG | M,V 882 | XP_011543675.1 | |
| XM_011545375.1 | 1016 | Missense Mutation | ATG,GTG | M,V 874 | XP_011543677.1 | |
| XM_011545385.1 | 1016 | Missense Mutation | ATG,GTG | M,V 151 | XP_011543687.1 | |
| XM_017018563.1 | 1016 | Missense Mutation | ATG,GTG | M,V 879 | XP_016874052.1 | |
| XM_017018564.1 | 1016 | Missense Mutation | ATG,GTG | M,V 878 | XP_016874053.1 | |
| XM_017018565.1 | 1016 | Missense Mutation | ATG,GTG | M,V 877 | XP_016874054.1 | |
| XM_017018566.1 | 1016 | Missense Mutation | ATG,GTG | M,V 865 | XP_016874055.1 | |
| XM_017018567.1 | 1016 | Missense Mutation | ATG,GTG | M,V 889 | XP_016874056.1 | |
| XM_017018568.1 | 1016 | Missense Mutation | ATG,GTG | M,V 886 | XP_016874057.1 | |
| XM_017018569.1 | 1016 | Missense Mutation | ATG,GTG | M,V 855 | XP_016874058.1 | |
| XM_017018570.1 | 1016 | Missense Mutation | ATG,GTG | M,V 889 | XP_016874059.1 | |
| XM_017018571.1 | 1016 | Missense Mutation | ATG,GTG | M,V 886 | XP_016874060.1 | |
| XM_017018572.1 | 1016 | Missense Mutation | ATG,GTG | M,V 654 | XP_016874061.1 | |
| XM_017018573.1 | 1016 | Missense Mutation | ATG,GTG | M,V 877 | XP_016874062.1 | |
| XM_017018574.1 | 1016 | Missense Mutation | ATG,GTG | M,V 644 | XP_016874063.1 | |
| XM_017018575.1 | 1016 | Missense Mutation | ATG,GTG | M,V 643 | XP_016874064.1 | |
| XM_017018576.1 | 1016 | Missense Mutation | ATG,GTG | M,V 470 | XP_016874065.1 | |
| XM_017018577.1 | 1016 | Missense Mutation | ATG,GTG | M,V 148 | XP_016874066.1 | |
| XM_017018578.1 | 1016 | Missense Mutation | ATG,GTG | M,V 886 | XP_016874067.1 | |
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