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CCTTGATATTTTCAGTTGCCCCCAC[A/G]ACTAACTGGTGAATGCTGTCAATCT
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 | |||
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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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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 | 1020 | Silent Mutation | GTC,GTT | V,V 288 | NP_058626.1 | |
XM_011513480.1 | 1020 | Silent Mutation | GTC,GTT | V,V 319 | XP_011511782.1 | |
XM_011513483.1 | 1020 | Silent Mutation | GTC,GTT | V,V 286 | XP_011511785.1 | |
XM_011513485.2 | 1020 | Silent Mutation | GTC,GTT | V,V 207 | XP_011511787.1 | |
XM_017008296.1 | 1020 | Intron | XP_016863785.1 | |||
XM_017008297.1 | 1020 | Silent Mutation | GTC,GTT | V,V 238 | XP_016863786.1 | |
XM_017008298.1 | 1020 | Intron | XP_016863787.1 |