Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCACGATGCCTGCCACGGTGCCCC[C/T]GACGATGGCGGCGATGTTGGGGCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600065 | ||||||||||||||||||||
Literature Links: |
ITGB2 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 |
ITGB2 - integrin subunit beta 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000211.4 | 2366 | Missense Mutation | AGG,GGG | R,G 706 | NP_000202.3 | |
NM_001127491.2 | 2366 | Missense Mutation | AGG,GGG | R,G 706 | NP_001120963.2 | |
NM_001303238.1 | 2366 | Missense Mutation | AGG,GGG | R,G 637 | NP_001290167.1 | |
XM_006724001.1 | 2366 | Missense Mutation | AGG,GGG | R,G 637 | XP_006724064.1 | |
XM_017028341.1 | 2366 | Missense Mutation | AGG,GGG | R,G 637 | XP_016883830.1 |