Product Details

SNP ID
rs77539990
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:31561516 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGGCGGGGCCACTGCCCCGCTTG[G/T]GGGAAGCCGAGCGATGGTTTGTGGG
Phenotype
MIM: 613621
Polymorphism
G/T, Transversion 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_001201573.1 118 Intron NP_001188502.1
NM_001201574.1 118 Intron NP_001188503.1
NM_025152.2 118 Missense Mutation GGG,GTG G26V NP_079428.2
XM_011537181.2 118 Intron XP_011535483.1
XM_011537182.2 118 UTR 5 XP_011535484.1
XM_011537183.2 118 Missense Mutation GGG,GTG G26V XP_011535485.1
XM_011537184.2 118 Intron XP_011535486.1
XM_017021664.1 118 Missense Mutation GGG,GTG G26V XP_016877153.1
XM_017021665.1 118 Missense Mutation GGG,GTG G26V XP_016877154.1
XM_017021666.1 118 Missense Mutation GGG,GTG G26V XP_016877155.1
XM_017021667.1 118 UTR 5 XP_016877156.1

View Full Product Details