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CGGCAGACTATTGTCAAACTGGGGA[A/G]TAAAGTCCAGGAGTTGGAGAAACAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 186591 | ||||||||||||||||||||
Literature Links: |
LOC101928762 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 |
LOC101928762 - uncharacterized LOC101928762 | ||||||
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There are no transcripts associated with this gene. |
STX4 - syntaxin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272095.1 | 485 | UTR 5 | NP_001259024.1 | |||
NM_001272096.1 | 485 | Missense Mutation | AAT,AGT | N,S 55 | NP_001259025.1 | |
NM_004604.4 | 485 | Missense Mutation | AAT,AGT | N,S 57 | NP_004595.2 | |
XM_005255521.1 | 485 | Missense Mutation | AAT,AGT | N,S 53 | XP_005255578.1 | |
XM_011545925.2 | 485 | Intron | XP_011544227.1 |