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- SNP ID:
- rs79629431
- Gene
-
ALS2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.2: 201774266 - 201774266 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
AGCCAAAGTCCCAGACAAAGTGAAG[G/A]AGGATGCCATCCAGAATATATGTGG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606352
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Literature Links: |
ALS2 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
|
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AMR
|
| ALS2 - ALS2, alsin Rho guanine nucleotide exchange factor | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001135745.1 | Intron | NP_001129217.1 | ||||
| NM_020919.3 | Intron | NP_065970.2 | ||||
| XM_006712654.2 | Intron | XP_006712717.1 | ||||
| XM_006712655.3 | Intron | XP_006712718.1 | ||||
| XM_011511530.2 | Intron | XP_011509832.1 | ||||
| XM_017004569.1 | Intron | XP_016860058.1 | ||||
| XM_017004570.1 | Intron | XP_016860059.1 | ||||
| XM_017004571.1 | Intron | XP_016860060.1 | ||||
| XM_017004572.1 | Intron | XP_016860061.1 | ||||
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