Product Details

SNP ID
rs147914081
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:7573252 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGATCTTAGAAAATTTGAGAAGCC[A/G]GTTTTGACATTGACTGAGCAACCAA
Phenotype
MIM: 615359
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC101927391 PubMed Links

Gene Details

Gene
LOC101927391
Gene Name
uncharacterized LOC101927391
There are no transcripts associated with this gene.

Gene
MIOS
Gene Name
meiosis regulator for oocyte development
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019005.3 911 Silent Mutation CCA,CCG P259P NP_061878.3
XM_005249780.3 911 Silent Mutation CCA,CCG P259P XP_005249837.1
XM_005249781.3 911 Silent Mutation CCA,CCG P259P XP_005249838.1
XM_005249782.3 911 Silent Mutation CCA,CCG P259P XP_005249839.1
XM_005249784.3 911 Silent Mutation CCA,CCG P259P XP_005249841.1
XM_011515432.2 911 Silent Mutation CCA,CCG P259P XP_011513734.1
XM_017012361.1 911 Silent Mutation CCA,CCG P259P XP_016867850.1
XM_017012362.1 911 UTR 5 XP_016867851.1

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