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- SNP ID:
- rs79089091
- Gene
-
LOC100507283MSANTD2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 124799040 - 124799040 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
ATTTCTAGCCCAAATTAAGCCTCTG[C/T]ATTTAAACATGCAGGTACACAAGGA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
LOC100507283 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| LOC100507283 - uncharacterized LOC100507283 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| MSANTD2 - Myb/SANT DNA binding domain containing 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001308027.1 | Intron | NP_001294956.1 | ||||
| NM_001312919.1 | Intron | NP_001299848.1 | ||||
| NM_001312920.1 | Intron | NP_001299849.1 | ||||
| NM_001312921.1 | Intron | NP_001299850.1 | ||||
| NM_024631.3 | Intron | NP_078907.2 | ||||
| XM_005271674.3 | Intron | XP_005271731.3 | ||||
| XM_006718905.1 | Intron | XP_006718968.1 | ||||
| XM_006718906.3 | Intron | XP_006718969.1 | ||||
| XM_011542981.2 | Intron | XP_011541283.2 | ||||
| XM_011542982.2 | Intron | XP_011541284.2 | ||||
| XM_017018295.1 | Intron | XP_016873784.1 | ||||
| XM_017018296.1 | Intron | XP_016873785.1 | ||||
| XM_017018297.1 | Intron | XP_016873786.1 | ||||
| XM_017018298.1 | Intron | XP_016873787.1 | ||||
| XM_017018299.1 | Intron | XP_016873788.1 | ||||
| XM_017018300.1 | Intron | XP_016873789.1 | ||||
| XM_017018301.1 | Intron | XP_016873790.1 | ||||
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