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SNP ID

rs141349380

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:943354 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTCTGCAGCTTCGTGGGGGGCCTG[G/T]CTGGCTGTGGAGAGTACACTCGGGT

Phenotype

MIM: 610770 MIM: 616765

Polymorphism

G/T, Transversion 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	1746	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	1746	Missense Mutation	GCT,TCT	A556S	NP_689699.2

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