Product Details

SNP ID
rs200389697
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:33209360 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTTCTCCAGAACACTCCCAGAAA[C/G]AAAATGGGCACCCCCGTAAGGATGA
Phenotype
MIM: 603159 MIM: 607959
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
LRP3 PubMed Links

Gene Details

Gene
LRP3
Gene Name
LDL receptor related protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002333.3 1171 Intron NP_002324.2
XM_005258945.1 1171 Intron XP_005259002.1
Gene
SLC7A10
Gene Name
solute carrier family 7 member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019849.2 1171 Missense Mutation TTC,TTG F463L NP_062823.1
XM_006723284.2 1171 Missense Mutation TTC,TTG F384L XP_006723347.1
XM_011527119.1 1171 Missense Mutation TTC,TTG F600L XP_011525421.1
XM_011527120.1 1171 Missense Mutation TTC,TTG F573L XP_011525422.1

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