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- SNP ID:
- rs779325635
- Gene
-
STAG2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.X: 124000075 - 124000075 on Build GRCh38
- Polymorphism:
- A/T, Transversion substitution
- Context Sequence [VIC/FAM]:
AGCTCACCCTCCTTTTATATAAACT[A/T]CAGTCATGTGCTGAATAATGACGTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300826
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Literature Links: |
STAG2 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 |
| STAG2 - stromal antigen 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001042749.2 | Intron | NP_001036214.1 | ||||
| NM_001042750.1 | Intron | NP_001036215.1 | ||||
| NM_001042751.1 | Intron | NP_001036216.1 | ||||
| NM_001282418.1 | Intron | NP_001269347.1 | ||||
| NM_006603.4 | Intron | NP_006594.3 | ||||
| XM_005262357.2 | Intron | XP_005262414.1 | ||||
| XM_005262358.2 | Intron | XP_005262415.1 | ||||
| XM_005262359.3 | Intron | XP_005262416.1 | ||||
| XM_005262360.2 | Intron | XP_005262417.1 | ||||
| XM_005262361.2 | Intron | XP_005262418.1 | ||||
| XM_006724727.1 | Intron | XP_006724790.1 | ||||
| XM_006724728.3 | Intron | XP_006724791.1 | ||||
| XM_011531253.2 | Intron | XP_011529555.1 | ||||
| XM_017029232.1 | Intron | XP_016884721.1 | ||||
| XM_017029233.1 | Intron | XP_016884722.1 | ||||
| XM_017029234.1 | Intron | XP_016884723.1 | ||||
| XM_017029235.1 | Intron | XP_016884724.1 | ||||
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