Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCGTGGTCCAGCTTCAGGGATCCA[A/G]GTGAGACCCTTAGATGGAGCCCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 120980 | ||||||||||||||||||||
Literature Links: |
ITGAM 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 |
ITGAM - integrin subunit alpha M | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000632.3 | 232 | Missense Mutation | AAG,AGG | K,R 45 | NP_000623.2 | |
NM_001145808.1 | 232 | Missense Mutation | AAG,AGG | K,R 45 | NP_001139280.1 | |
XM_006721045.1 | 232 | Missense Mutation | AAG,AGG | K,R 45 | XP_006721108.1 | |
XM_011545850.2 | 232 | Intron | XP_011544152.1 | |||
XM_011545851.2 | 232 | Missense Mutation | AAG,AGG | K,R 45 | XP_011544153.1 | |
XM_017023216.1 | 232 | Missense Mutation | AAG,AGG | K,R 45 | XP_016878705.1 |