Product Details

SNP ID
rs6893500
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:178138361 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTCCGGAAGGACGATGATGAGGAT[A/G]TTGGTACCTGCATCTGTAGGCCTCC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RMND5B PubMed Links

Gene Details

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_001288794.1 917 Intron NP_001275723.1
NM_001288795.1 917 Intron NP_001275724.1
NM_022762.4 917 Intron NP_073599.2
XM_005265969.3 917 Intron XP_005266026.1
XM_005265971.4 917 UTR 5 XP_005266028.1
XM_005265972.3 917 UTR 5 XP_005266029.1
XM_017009727.1 917 Intron XP_016865216.1
XM_017009728.1 917 Intron XP_016865217.1

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