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CTACGATCTTCCAGGAGGATGCAGG[C/T]GGCTTTGGGCAGAGCGTGGTGCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602453 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ITGAD 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ITGAD - integrin subunit alpha D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318185.1 | 226 | Silent Mutation | GGC,GGT | G,G 33 | NP_001305114.1 | |
NM_005353.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | NP_005344.2 | |
XM_011545835.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544137.1 | |
XM_011545836.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544138.1 | |
XM_011545837.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544139.1 | |
XM_011545838.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544140.1 | |
XM_011545839.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544141.1 | |
XM_011545841.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544143.1 | |
XM_011545842.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544144.1 | |
XM_011545843.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544145.1 | |
XM_011545844.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544146.1 | |
XM_011545845.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544147.1 | |
XM_011545846.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544148.1 | |
XM_011545847.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544149.1 | |
XM_011545848.2 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_011544150.1 | |
XM_017023215.1 | 226 | Silent Mutation | GGC,GGT | G,G 33 | XP_016878704.1 |