Product Details

SNP ID
rs200401432
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:31562125 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGAAGAACACAAATCATGTCCCGA[A/G]GACTTCCAAAGCAGAAACCGATAGA
Phenotype
MIM: 613621
Polymorphism
A/G, 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_001201573.1 207 Intron NP_001188502.1
NM_001201574.1 207 Intron NP_001188503.1
NM_025152.2 207 Missense Mutation AGA,GGA R56G NP_079428.2
XM_011537181.2 207 Intron XP_011535483.1
XM_011537182.2 207 UTR 5 XP_011535484.1
XM_011537183.2 207 Missense Mutation AGA,GGA R56G XP_011535485.1
XM_011537184.2 207 Intron XP_011535486.1
XM_017021664.1 207 Missense Mutation AGA,GGA R56G XP_016877153.1
XM_017021665.1 207 Missense Mutation AGA,GGA R56G XP_016877154.1
XM_017021666.1 207 Missense Mutation AGA,GGA R56G XP_016877155.1
XM_017021667.1 207 UTR 5 XP_016877156.1

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