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- SNP ID:
- rs369105868
- Gene
-
IPO9-AS1MIR1231NAV1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 201803608 - 201803608 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
TTGGCCCTAGAACTTCGGATCAAGA[G/T]ACAAAACTCCTCAGATAGCATCTCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
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Phenotype: |
MIM: 611628
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Literature Links: |
IPO9-AS1 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 |
| IPO9-AS1 - IPO9 antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| MIR1231 - microRNA 1231 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| NAV1 - neuron navigator 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001167738.1 | 3388 | Missense Mutation | AGA,ATA | R,I 787 | NP_001161210.1 | |
| NM_020443.4 | 3388 | Missense Mutation | AGA,ATA | R,I 1178 | NP_065176.3 | |
| XM_006711609.2 | 3388 | Missense Mutation | AGA,ATA | R,I 787 | XP_006711672.2 | |
| XM_006711610.2 | 3388 | Missense Mutation | AGA,ATA | R,I 779 | XP_006711673.2 | |
| XM_006711611.1 | 3388 | Missense Mutation | AGA,ATA | R,I 686 | XP_006711674.1 | |
| XM_011510097.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1178 | XP_011508399.1 | |
| XM_011510098.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1170 | XP_011508400.1 | |
| XM_011510099.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1170 | XP_011508401.1 | |
| XM_011510100.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1121 | XP_011508402.1 | |
| XM_011510101.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1113 | XP_011508403.1 | |
| XM_011510102.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1113 | XP_011508404.1 | |
| XM_017002751.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1121 | XP_016858240.1 | |
| XM_017002752.1 | 3388 | Missense Mutation | AGA,ATA | R,I 779 | XP_016858241.1 | |
| XM_017002753.1 | 3388 | Missense Mutation | AGA,ATA | R,I 1170 | XP_016858242.1 | |
| XM_017002754.1 | 3388 | Intron | XP_016858243.1 | |||
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