Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGAGCCACACCGAGAACCGCCGCG[A/G]AGCCCTCATCCCTAACGGTGAAAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608314 MIM: 610981 | ||||||||||||||||||||
Literature Links: |
SEPT3 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 |
SEPT3 - septin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019106.5 | 132 | Intron | NP_061979.3 | |||
NM_145733.2 | 132 | Intron | NP_663786.2 | |||
XM_017028862.1 | 132 | Intron | XP_016884351.1 |
WBP2NL - WBP2 N-terminal like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152613.2 | 132 | Missense Mutation | GAA,GGA | E,G 13 | NP_689826.2 |