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- SNP ID:
- rs139362546
- Gene
-
ST7ST7-AS1ST7-OT4 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.7: 116953639 - 116953639 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
CCGTGTGGTTCTTCATCGTGCTATT[C/G]CTGGTCTACATCCTGCGGGTGCCTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600833
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Literature Links: |
ST7 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 |
| ST7 - suppression of tumorigenicity 7 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_018412.3 | 313 | Missense Mutation | TTC,TTG | F,L 33 | NP_060882.2 | |
| NM_021908.2 | 313 | Missense Mutation | TTC,TTG | F,L 33 | NP_068708.1 | |
| ST7-AS1 - ST7 antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| ST7-OT4 - ST7 overlapping transcript 4 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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