Product Details

SNP ID

rs144453653

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:943329 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGTCACCAAGTGGACCGTGGATGA[C/T]GTCTGCAGCTTCGTGGGGGGCCTGT

Phenotype

MIM: 610770 MIM: 616765

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NOC2L PubMed Links

Gene Details

Gene

NOC2L

Gene Name

NOC2 like nucleolar associated transcriptional repressor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015658.3	1721	Intron			NP_056473.2

Gene

SAMD11

Gene Name

sterile alpha motif domain containing 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152486.2	1721	Silent Mutation	GAC,GAT	D547D	NP_689699.2

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