Product Details

SNP ID
rs35433432
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:31565047 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACTTGCACTAGCAGCGAACGATT[C/T]GGTAGGTGTTTATTAATAGAAATAT
Phenotype
MIM: 613621
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NUBPL PubMed Links

Gene Details

Gene
NUBPL
Gene Name
nucleotide binding protein like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001201573.1 331 Intron NP_001188502.1
NM_001201574.1 331 Intron NP_001188503.1
NM_025152.2 331 Missense Mutation TCG,TTG S97L NP_079428.2
XM_011537181.2 331 Intron XP_011535483.1
XM_011537182.2 331 UTR 5 XP_011535484.1
XM_011537183.2 331 Missense Mutation TCG,TTG S97L XP_011535485.1
XM_011537184.2 331 Intron XP_011535486.1
XM_017021664.1 331 Missense Mutation TCG,TTG S97L XP_016877153.1
XM_017021665.1 331 Missense Mutation TCG,TTG S97L XP_016877154.1
XM_017021666.1 331 Missense Mutation TCG,TTG S97L XP_016877155.1
XM_017021667.1 331 UTR 5 XP_016877156.1

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