Product Details

SNP ID
rs201096086
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:30472872 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTGCATCACTGTGATGGCCATGG[C/T]GCTGCTGTCTGGGTTCTTTTTCTTC
Phenotype
MIM: 153370
Polymorphism
C/T, 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_001114380.1 211 Missense Mutation GCG,GTG A12V NP_001107852.1
NM_002209.2 211 Missense Mutation GCG,GTG A12V NP_002200.2
XM_005255313.1 211 Missense Mutation GCG,GTG A12V XP_005255370.1
XM_006721044.1 211 Missense Mutation GCG,GTG A12V XP_006721107.1
XM_011545849.1 211 UTR 5 XP_011544151.1

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