Product Details

SNP ID
rs141980234
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35250465 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGTACAAGTCTTTCTGCCGGGACC[C/G]CATCGCCGATGCCTTCTCCCCGGCC
Phenotype
MIM: 616582
Polymorphism
C/G, Transversion 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_001260489.1 627 Missense Mutation CCC,CGC P135R NP_001247418.1
NM_001260490.1 627 Missense Mutation CCC,CGC P135R NP_001247419.1
NM_015925.6 627 Missense Mutation CCC,CGC P135R NP_057009.3
NM_205834.3 627 Missense Mutation CCC,CGC P135R NP_991403.1
NM_205835.3 627 Missense Mutation CCC,CGC P135R NP_991404.1
XM_005258980.1 627 Missense Mutation CCC,CGC P135R XP_005259037.1
XM_005258982.1 627 Missense Mutation CCC,CGC P135R XP_005259039.1
XM_011527026.1 627 Missense Mutation CCC,CGC P135R XP_011525328.1

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