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SNP ID

rs192170316

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:178150976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTATACCTCAATGGGCAGTGTGTCT[C/T]CTGCCAAAACCATGATCCTGAAATG

Phenotype

MIM: 606470

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NHP2 PubMed Links

Gene Details

Gene

NHP2

Gene Name

NHP2 ribonucleoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001034833.1		Intron			NP_001030005.1
NM_017838.3		Intron			NP_060308.1

Gene

RMND5B

Gene Name

required for meiotic nuclear division 5 homolog B

There are no transcripts associated with this gene.

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