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CCTTAATCAGAGCCCCCCATGCCCT[C/T]TGCAGCTCAGAGTCGTCTTCCTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604682 MIM: 616624 | ||||||||||||||||||||
Literature Links: |
ITGAE 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 |
ITGAE - integrin subunit alpha E | ||||||
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There are no transcripts associated with this gene. |
NCBP3 - nuclear cap binding subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114118.2 | 1679 | Silent Mutation | CAA,CAG | Q,Q 578 | NP_001107590.1 | |
XM_005256717.2 | 1679 | Silent Mutation | CAA,CAG | Q,Q 578 | XP_005256774.1 | |
XM_006721556.2 | 1679 | Silent Mutation | CAA,CAG | Q,Q 443 | XP_006721619.1 | |
XM_011523954.2 | 1679 | Silent Mutation | CAA,CAG | Q,Q 464 | XP_011522256.1 | |
XM_011523955.2 | 1679 | Silent Mutation | CAA,CAG | Q,Q 443 | XP_011522257.1 | |
XM_017024826.1 | 1679 | Silent Mutation | CAA,CAG | Q,Q 443 | XP_016880315.1 | |
XM_017024827.1 | 1679 | Silent Mutation | CAA,CAG | Q,Q 298 | XP_016880316.1 | |
XM_017024828.1 | 1679 | Silent Mutation | CAA,CAG | Q,Q 298 | XP_016880317.1 | |
XM_017024829.1 | 1679 | Silent Mutation | CAA,CAG | Q,Q 298 | XP_016880318.1 |