Product Details

SNP ID

rs10143899

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:31562923 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCGCCCTGCCTACTAGCTCATTTTT[C/T]CCCATTTTTATCAGAAGGGAATTCT

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		Intron			NP_001188502.1
NM_001201574.1		Intron			NP_001188503.1
NM_025152.2		Intron			NP_079428.2
XM_011537181.2		Intron			XP_011535483.1
XM_011537182.2		Intron			XP_011535484.1
XM_011537183.2		Intron			XP_011535485.1
XM_011537184.2		Intron			XP_011535486.1
XM_017021664.1		Intron			XP_016877153.1
XM_017021665.1		Intron			XP_016877154.1
XM_017021666.1		Intron			XP_016877155.1
XM_017021667.1		Intron			XP_016877156.1

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