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- SNP ID:
- rs763855018
- Gene
-
SEPT9 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.17: 77469373 - 77469373 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
TGAGGAAAGGAAGGGCTGGGTGGTC[G/A]TCATTCCCTGCAGCTAGGAGGCAAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604061
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Literature Links: |
SEPT9 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 |
| SEPT9 - septin 9 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001113491.1 | Intron | NP_001106963.1 | ||||
| NM_001113492.1 | Intron | NP_001106964.1 | ||||
| NM_001113493.1 | Intron | NP_001106965.1 | ||||
| NM_001113494.1 | Intron | NP_001106966.1 | ||||
| NM_001113495.1 | Intron | NP_001106967.1 | ||||
| NM_001113496.1 | Intron | NP_001106968.1 | ||||
| NM_001293695.1 | Intron | NP_001280624.1 | ||||
| NM_001293696.1 | Intron | NP_001280625.1 | ||||
| NM_001293697.1 | Intron | NP_001280626.1 | ||||
| NM_001293698.1 | Intron | NP_001280627.1 | ||||
| NM_006640.4 | Intron | NP_006631.2 | ||||
| XM_005256962.1 | Intron | XP_005257019.1 | ||||
| XM_006721643.2 | Intron | XP_006721706.1 | ||||
| XM_006721644.1 | Intron | XP_006721707.1 | ||||
| XM_011524204.1 | Intron | XP_011522506.1 | ||||
| XM_011524206.1 | Intron | XP_011522508.1 | ||||
| XM_011524207.1 | Intron | XP_011522509.1 | ||||
| XM_011524208.2 | Intron | XP_011522510.1 | ||||
| XM_017024031.1 | Intron | XP_016879520.1 | ||||
| XM_017024032.1 | Intron | XP_016879521.1 | ||||
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