Product Details

SNP ID
rs113477430
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:178142872 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCAGAACTTCGACTCTGAGATCTG[C/T]GGTGTTGTGTCAGATGCGGTGTGGG
Phenotype
MIM: 606470
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NHP2 PubMed Links

Gene Details

Gene
NHP2
Gene Name
NHP2 ribonucleoprotein
There are no transcripts associated with this gene.

Gene
RMND5B
Gene Name
required for meiotic nuclear division 5 homolog B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288794.1 552 Silent Mutation TGC,TGT C102C NP_001275723.1
NM_001288795.1 552 Silent Mutation TGC,TGT C89C NP_001275724.1
NM_022762.4 552 Silent Mutation TGC,TGT C102C NP_073599.2
XM_005265969.3 552 Silent Mutation TGC,TGT C102C XP_005266026.1
XM_005265971.4 552 Silent Mutation TGC,TGT C42C XP_005266028.1
XM_005265972.3 552 Silent Mutation TGC,TGT C42C XP_005266029.1
XM_017009727.1 552 Silent Mutation TGC,TGT C102C XP_016865216.1
XM_017009728.1 552 Silent Mutation TGC,TGT C42C XP_016865217.1

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