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GCTCTTCAGTTCTTGCCACCTGGTG[G/T]TCTTTCCCTCATTAATCAGGGACAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 615463 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SZT2 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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SZT2 - seizure threshold 2 homolog (mouse) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015284.3 | Intron | NP_056099.3 | ||||
XM_005270686.3 | Intron | XP_005270743.1 | ||||
XM_006710501.3 | Intron | XP_006710564.1 | ||||
XM_011541106.2 | Intron | XP_011539408.1 | ||||
XM_011541107.2 | Intron | XP_011539409.1 | ||||
XM_017000819.1 | Intron | XP_016856308.1 | ||||
XM_017000820.1 | Intron | XP_016856309.1 | ||||
XM_017000821.1 | Intron | XP_016856310.1 |