Product Details

SNP ID

rs144364133

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:156949921 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCACGCGACTTCGGAAGGCGAGGCT[C/T]CCGGGGGTTGCGAGGGGCGCGGCGC

Phenotype

MIM: 611269

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NOM1 PubMed Links

Gene Details

Gene

NOM1

Gene Name

nucleolar protein with MIF4G domain 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138400.1	199	Missense Mutation	CCC,TCC	P62S	NP_612409.1

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