Product Details

SNP ID

rs74401893

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:67720753 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTAAACTAGGTTAATCTTGAAAGT[C/T]CTTTCCAGTTCTAAATGTCTAAATA

Phenotype

MIM: 615366

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NOL11 PubMed Links

Gene Details

Gene

NOL11

Gene Name

nucleolar protein 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303272.1		Intron			NP_001290201.1
NM_015462.4		Intron			NP_056277.2

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