Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACTGGCTCCTGTCCCCTAGGCCT[A/G]TGGTCCCACCGTGCACCAGACTTGC
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
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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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 | 208 | Missense Mutation | TAT,TGT | Y,C 105 | NP_000623.2 | |
NM_001145808.1 | 208 | Missense Mutation | TAT,TGT | Y,C 105 | NP_001139280.1 | |
XM_006721045.1 | 208 | Missense Mutation | TAT,TGT | Y,C 105 | XP_006721108.1 | |
XM_011545850.2 | 208 | Missense Mutation | TAT,TGT | Y,C 43 | XP_011544152.1 | |
XM_011545851.2 | 208 | Missense Mutation | TAT,TGT | Y,C 105 | XP_011544153.1 | |
XM_017023216.1 | 208 | Missense Mutation | TAT,TGT | Y,C 105 | XP_016878705.1 |