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TGTGTCCCCAAGGCTGGAATCATGG[G/T]GGCACGATCATAGCTCACTGTAGCC
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 - Not Available | Caucasian - Not Available | CEPH (CEU)
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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 |
ITGAL - integrin subunit alpha L | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114380.1 | Intron | NP_001107852.1 | ||||
NM_002209.2 | Intron | NP_002200.2 | ||||
XM_005255313.1 | Intron | XP_005255370.1 | ||||
XM_006721044.1 | Intron | XP_006721107.1 | ||||
XM_011545849.1 | Intron | XP_011544151.1 |
Set Membership: |
HapMap |