Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 153370 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ITGAL PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ITGAL - integrin subunit alpha L | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114380.1 | 816 | Missense Mutation | CGG,TGG | R,W 131 | NP_001107852.1 | |
NM_002209.2 | 816 | Missense Mutation | CGG,TGG | R,W 214 | NP_002200.2 | |
XM_005255313.1 | 816 | Missense Mutation | CGG,TGG | R,W 214 | XP_005255370.1 | |
XM_006721044.1 | 816 | Missense Mutation | CGG,TGG | R,W 131 | XP_006721107.1 | |
XM_011545849.1 | 816 | Missense Mutation | CGG,TGG | R,W 118 | XP_011544151.1 |
Set Membership: |
HapMap |