Product Details

SNP ID
rs150283228
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:115962741 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCCGCCTTGTACGGCCACTGCGAG[A/C]GCGTCCCACCGTCGGAGCTGCCTGG
Phenotype
MIM: 610046
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
LVRN PubMed Links

Gene Details

Gene
LVRN
Gene Name
laeverin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173800.4 302 Missense Mutation AGC,CGC S42R NP_776161.3
XM_011543263.2 302 Missense Mutation AGC,CGC S42R XP_011541565.1
XM_011543264.2 302 Missense Mutation AGC,CGC S42R XP_011541566.1
XM_017009215.1 302 Missense Mutation AGC,CGC S42R XP_016864704.1

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