Search Thermo Fisher Scientific
- SNP ID:
- rs28544456
- Gene
-
ASCC2 - Gene Name
- activating signal cointegrator 1 complex subunit 2
- Set Membership:
- -
- Chromosome Location:
- Chr.22: 29789057 - 29789057 on Build GRCh38
- Polymorphism:
- A/T, Transversion substitution
- Context Sequence [VIC/FAM]:
TTGCTCCTCTTGCGGTCGGCCATGG[A/T]TCTCCGGTTGTGGTTGGCTCTTGTC
Genomic Map
Back To TopAssay Details
Species: |
Human |
dbSNP Submissions: |
NA
|
Phenotype: |
MIM: 614216
|
Literature Links: |
ASCC2 PubMed Links |
Allele Nomenclature: |
|
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 |
| ASCC2 - activating signal cointegrator 1 complex subunit 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001242906.1 | 2414 | Missense Mutation | ACC,TCC | T,S 668 | NP_001229835.1 | |
| NM_032204.4 | 2414 | Missense Mutation | ACC,TCC | T,S 744 | NP_115580.2 | |
| XM_005261775.2 | 2414 | Missense Mutation | ACC,TCC | T,S 744 | XP_005261832.1 | |
| XM_011530442.2 | 2414 | Missense Mutation | ACC,TCC | T,S 749 | XP_011528744.1 | |
| XM_011530443.2 | 2414 | Missense Mutation | ACC,TCC | T,S 749 | XP_011528745.1 | |
| XM_011530444.2 | 2414 | Missense Mutation | ACC,TCC | T,S 749 | XP_011528746.1 | |
| XM_011530445.2 | 2414 | Missense Mutation | ACC,TCC | T,S 749 | XP_011528747.1 | |
| XM_011530446.2 | 2414 | Missense Mutation | ACC,TCC | T,S 749 | XP_011528748.1 | |
| XM_011530448.2 | 2414 | Missense Mutation | ACC,TCC | T,S 696 | XP_011528750.1 | |
| XM_011530449.2 | 2414 | Missense Mutation | ACC,TCC | T,S 696 | XP_011528751.1 | |
| XM_011530450.2 | 2414 | Missense Mutation | ACC,TCC | T,S 635 | XP_011528752.1 | |
| XM_011530451.2 | 2414 | Missense Mutation | ACC,TCC | T,S 635 | XP_011528753.1 | |
| XM_011530452.2 | 2414 | Missense Mutation | ACC,TCC | T,S 635 | XP_011528754.1 | |
| XM_011530453.2 | 2414 | Missense Mutation | ACC,TCC | T,S 635 | XP_011528755.1 | |
| XM_011530454.2 | 2414 | Missense Mutation | ACC,TCC | T,S 635 | XP_011528756.1 | |
| XM_011530455.2 | 2414 | Missense Mutation | ACC,TCC | T,S 635 | XP_011528757.1 | |
| XM_017028991.1 | 2414 | Missense Mutation | ACC,TCC | T,S 803 | XP_016884480.1 | |
| XM_017028992.1 | 2414 | Missense Mutation | ACC,TCC | T,S 798 | XP_016884481.1 | |
| XM_017028993.1 | 2414 | Missense Mutation | ACC,TCC | T,S 778 | XP_016884482.1 | |
| XM_017028994.1 | 2414 | Missense Mutation | ACC,TCC | T,S 773 | XP_016884483.1 | |
| XM_017028995.1 | 2414 | Missense Mutation | ACC,TCC | T,S 750 | XP_016884484.1 | |
| XM_017028996.1 | 2414 | Missense Mutation | ACC,TCC | T,S 749 | XP_016884485.1 | |
| XM_017028997.1 | 2414 | Missense Mutation | ACC,TCC | T,S 745 | XP_016884486.1 | |
| XM_017028998.1 | 2414 | Missense Mutation | ACC,TCC | T,S 744 | XP_016884487.1 | |
| XM_017028999.1 | 2414 | Missense Mutation | ACC,TCC | T,S 744 | XP_016884488.1 | |
| XM_017029000.1 | 2414 | Missense Mutation | ACC,TCC | T,S 744 | XP_016884489.1 | |
| XM_017029001.1 | 2414 | Missense Mutation | ACC,TCC | T,S 691 | XP_016884490.1 | |
| XM_017029002.1 | 2414 | Missense Mutation | ACC,TCC | T,S 691 | XP_016884491.1 | |
| XM_017029003.1 | 2414 | Missense Mutation | ACC,TCC | T,S 691 | XP_016884492.1 | |
| XM_017029004.1 | 2414 | Missense Mutation | ACC,TCC | T,S 666 | XP_016884493.1 | |
| XM_017029005.1 | 2414 | Missense Mutation | ACC,TCC | T,S 630 | XP_016884494.1 | |
| XM_017029006.1 | 2414 | Missense Mutation | ACC,TCC | T,S 630 | XP_016884495.1 | |
| XM_017029007.1 | 2414 | Missense Mutation | ACC,TCC | T,S 630 | XP_016884496.1 | |
| XM_017029008.1 | 2414 | Missense Mutation | ACC,TCC | T,S 630 | XP_016884497.1 | |
| XM_017029009.1 | 2414 | Missense Mutation | ACC,TCC | T,S 630 | XP_016884498.1 | |
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