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ACACGGCCCTCTCCACATAGTCTAC[C/T]GCGTGTTCCACATTGTACTCGATCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 186590 MIM: 615733 | ||||||||||||||||||||
Literature Links: |
STX1A 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 |
STX1A - syntaxin 1A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001165903.1 | 776 | Intron | NP_001159375.1 | |||
NM_004603.3 | 776 | Silent Mutation | GCA,GCG | A,A 240 | NP_004594.1 | |
XM_017012567.1 | 776 | Intron | XP_016868056.1 |
WBSCR22 - Williams-Beuren syndrome chromosome region 22 | ||||||
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There are no transcripts associated with this gene. |