Product Details

SNP ID
rs143978527
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35250528 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCTCAATGCCCAGCTGGCAGCCG[A/G]GAACCCAGGCTACAACCCCTACGTT
Phenotype
MIM: 616582
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LSR PubMed Links

Gene Details

Gene
LSR
Gene Name
lipolysis stimulated lipoprotein receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001260489.1 690 Missense Mutation GAG,GGG E156G NP_001247418.1
NM_001260490.1 690 Missense Mutation GAG,GGG E156G NP_001247419.1
NM_015925.6 690 Missense Mutation GAG,GGG E156G NP_057009.3
NM_205834.3 690 Missense Mutation GAG,GGG E156G NP_991403.1
NM_205835.3 690 Missense Mutation GAG,GGG E156G NP_991404.1
XM_005258980.1 690 Missense Mutation GAG,GGG E156G XP_005259037.1
XM_005258982.1 690 Missense Mutation GAG,GGG E156G XP_005259039.1
XM_011527026.1 690 Missense Mutation GAG,GGG E156G XP_011525328.1

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