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CTCCACCGTCTGTACCTCCTCCTCA[C/T]GGATCTCTGCTGGGAGGGGGATTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600566 MIM: 605577 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NRXN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NRXN2 - neurexin 2 | ||||||
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There are no transcripts associated with this gene. |
RASGRP2 - RAS guanyl releasing protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098670.1 | 2356 | Missense Mutation | NP_001092140.1 | |||
NM_001098671.1 | 2356 | Missense Mutation | NP_001092141.1 | |||
NM_001318398.1 | 2356 | Missense Mutation | NP_001305327.1 | |||
NM_153819.1 | 2356 | Missense Mutation | NP_722541.1 | |||
XM_005273707.3 | 2356 | Missense Mutation | XP_005273764.3 | |||
XM_011544718.1 | 2356 | Missense Mutation | XP_011543020.1 | |||
XM_011544720.1 | 2356 | Missense Mutation | XP_011543022.1 | |||
XM_011544721.1 | 2356 | Missense Mutation | XP_011543023.1 | |||
XM_011544722.1 | 2356 | Missense Mutation | XP_011543024.1 | |||
XM_011544723.2 | 2356 | Missense Mutation | XP_011543025.1 | |||
XM_011544725.2 | 2356 | Missense Mutation | XP_011543027.1 | |||
XM_017017082.1 | 2356 | Missense Mutation | XP_016872571.1 | |||
XM_017017083.1 | 2356 | Missense Mutation | XP_016872572.1 | |||
XM_017017084.1 | 2356 | Missense Mutation | XP_016872573.1 | |||
XM_017017085.1 | 2356 | Missense Mutation | XP_016872574.1 | |||
XM_017017086.1 | 2356 | Missense Mutation | XP_016872575.1 |