Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGACGGGACGGCTGTATGACTGC[A/G]CAGCTGCCACCGGCATGTGCCAGCC
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 |
---|---|---|
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 |
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 | 329 | Missense Mutation | ACA,GCA | T,A 68 | NP_001305114.1 | |
NM_005353.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | NP_005344.2 | |
XM_011545835.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544137.1 | |
XM_011545836.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544138.1 | |
XM_011545837.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544139.1 | |
XM_011545838.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544140.1 | |
XM_011545839.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544141.1 | |
XM_011545841.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544143.1 | |
XM_011545842.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544144.1 | |
XM_011545843.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544145.1 | |
XM_011545844.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544146.1 | |
XM_011545845.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544147.1 | |
XM_011545846.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544148.1 | |
XM_011545847.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544149.1 | |
XM_011545848.2 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_011544150.1 | |
XM_017023215.1 | 329 | Missense Mutation | ACA,GCA | T,A 68 | XP_016878704.1 |