Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGAAATCTCAACCACTCTCCCTT[C/T]GATTTGCCTTCATAAAAAGAACAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607645 MIM: 606046 | ||||||||||||||||||||
Literature Links: |
NSG1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NSG1 - neuron specific gene family member 1 | ||||||
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There are no transcripts associated with this gene. |
STX18 - syntaxin 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016930.2 | 925 | Missense Mutation | AAA,GAA | K,E 257 | NP_058626.1 | |
XM_011513480.1 | 925 | Missense Mutation | AAA,GAA | K,E 288 | XP_011511782.1 | |
XM_011513483.1 | 925 | Missense Mutation | AAA,GAA | K,E 255 | XP_011511785.1 | |
XM_011513485.2 | 925 | Missense Mutation | AAA,GAA | K,E 176 | XP_011511787.1 | |
XM_017008296.1 | 925 | Intron | XP_016863785.1 | |||
XM_017008297.1 | 925 | Missense Mutation | AAA,GAA | K,E 207 | XP_016863786.1 | |
XM_017008298.1 | 925 | Intron | XP_016863787.1 |