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TGTCGCCGAAGGCCTTGCCACAATG[C/T]GGGCACTTGTAGGGCTTCTGGCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 153370 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ITGAL 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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ITGAL - integrin subunit alpha L | ||||||
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There are no transcripts associated with this gene. |
ZNF747 - zinc finger protein 747 | ||||||
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There are no transcripts associated with this gene. |
ZNF768 - zinc finger protein 768 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024671.3 | 1045 | Silent Mutation | CCA,CCG | P,P 348 | NP_078947.3 | |
XM_017023665.1 | 1045 | Silent Mutation | CCA,CCG | P,P 372 | XP_016879154.1 | |
XM_017023666.1 | 1045 | Silent Mutation | CCA,CCG | P,P 317 | XP_016879155.1 |