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AGTGAGCAGTCCAGCTGGTTCATTG[G/T]TTGACACCGAGATTATGTGACTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607021 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SEZ6L PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
SEZ6L - seizure related 6 homolog like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184773.1 | Intron | NP_001171702.1 | ||||
NM_001184774.1 | Intron | NP_001171703.1 | ||||
NM_001184775.1 | Intron | NP_001171704.1 | ||||
NM_001184776.1 | Intron | NP_001171705.1 | ||||
NM_001184777.1 | Intron | NP_001171706.1 | ||||
NM_021115.4 | Intron | NP_066938.2 | ||||
XM_005261439.3 | Intron | XP_005261496.1 | ||||
XM_005261440.3 | Intron | XP_005261497.1 | ||||
XM_006724195.3 | Intron | XP_006724258.1 | ||||
XM_011530037.2 | Intron | XP_011528339.1 | ||||
XM_011530038.2 | Intron | XP_011528340.1 | ||||
XM_011530039.2 | Intron | XP_011528341.1 | ||||
XM_017028699.1 | Intron | XP_016884188.1 | ||||
XM_017028700.1 | Intron | XP_016884189.1 |