Product Details

SNP ID
rs201621684
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:7572733 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCAGTTGGACAAGCAAATGGTCG[A/C]GTTGTACTTACAAGCCTTGGTCAAG
Phenotype
MIM: 615359
Polymorphism
A/C, Transversion 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_019005.3 392 Silent Mutation CGA,CGC R86R NP_061878.3
XM_005249780.3 392 Silent Mutation CGA,CGC R86R XP_005249837.1
XM_005249781.3 392 Silent Mutation CGA,CGC R86R XP_005249838.1
XM_005249782.3 392 Silent Mutation CGA,CGC R86R XP_005249839.1
XM_005249784.3 392 Silent Mutation CGA,CGC R86R XP_005249841.1
XM_011515432.2 392 Silent Mutation CGA,CGC R86R XP_011513734.1
XM_017012361.1 392 Silent Mutation CGA,CGC R86R XP_016867850.1
XM_017012362.1 392 UTR 5 XP_016867851.1

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