Product Details
- SNP ID
-
rs140514685
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:64730141 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAAGCCCATGCGCCCCCCCAACACA[C/G]AGCTGGAGCGCAGGAAATAGGAAAC
- Phenotype
-
MIM: 600566
MIM: 605577
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
NRXN2
PubMed Links
Gene Details
- Gene
- NRXN2
- Gene Name
- neurexin 2
There are no transcripts associated with this gene.
- Gene
- RASGRP2
- Gene Name
- RAS guanyl releasing protein 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001098670.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
NP_001092140.1 |
NM_001098671.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
NP_001092141.1 |
NM_001318398.1 |
2044 |
Missense Mutation |
TCT,TGT |
S344C |
NP_001305327.1 |
NM_153819.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
NP_722541.1 |
XM_005273707.3 |
2044 |
Missense Mutation |
TCT,TGT |
S594C |
XP_005273764.3 |
XM_011544718.1 |
2044 |
Missense Mutation |
TCT,TGT |
S594C |
XP_011543020.1 |
XM_011544720.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
XP_011543022.1 |
XM_011544721.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
XP_011543023.1 |
XM_011544722.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
XP_011543024.1 |
XM_011544723.2 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
XP_011543025.1 |
XM_011544725.2 |
2044 |
Missense Mutation |
TCT,TGT |
S344C |
XP_011543027.1 |
XM_017017082.1 |
2044 |
Missense Mutation |
TCT,TGT |
S777C |
XP_016872571.1 |
XM_017017083.1 |
2044 |
Missense Mutation |
TCT,TGT |
S777C |
XP_016872572.1 |
XM_017017084.1 |
2044 |
Missense Mutation |
TCT,TGT |
S489C |
XP_016872573.1 |
XM_017017085.1 |
2044 |
Missense Mutation |
TCT,TGT |
S430C |
XP_016872574.1 |
XM_017017086.1 |
2044 |
Missense Mutation |
TCT,TGT |
S344C |
XP_016872575.1 |
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