Product Details

SNP ID
rs142110125
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:30479365 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGCAACGTAGACCTGGTATTTCT[A/G]TTTGATGGTTCGATGAGCTTGCAGC
Phenotype
MIM: 153370
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ITGAL PubMed Links

Gene Details

Gene
ITGAL
Gene Name
integrin subunit alpha L
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114380.1 656 Intron NP_001107852.1
NM_002209.2 656 Silent Mutation CTA,CTG L160L NP_002200.2
XM_005255313.1 656 Silent Mutation CTA,CTG L160L XP_005255370.1
XM_006721044.1 656 Intron XP_006721107.1
XM_011545849.1 656 Silent Mutation CTA,CTG L64L XP_011544151.1

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