Product Details

SNP ID

rs6952214

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:156950102 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCGGAGCCGAAGAAGCCAGCGGTC[A/C]CCGGCAGGACACGGAGGAGCGCGCC

Phenotype

MIM: 611269

Polymorphism

A/C, Transversion 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	380	Missense Mutation	CAC,CCC	H122P	NP_612409.1

View Full Product Details