Product Details

SNP ID
rs141631713
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:7573433 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACAATAATTGAAAGAAGTGTGCAA[C/T]CTTGTGACAATTACATTGCTTCCTT
Phenotype
MIM: 615359
Polymorphism
C/T, 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 1092 Missense Mutation CCT,TCT P320S NP_061878.3
XM_005249780.3 1092 Missense Mutation CCT,TCT P320S XP_005249837.1
XM_005249781.3 1092 Missense Mutation CCT,TCT P320S XP_005249838.1
XM_005249782.3 1092 Missense Mutation CCT,TCT P320S XP_005249839.1
XM_005249784.3 1092 Missense Mutation CCT,TCT P320S XP_005249841.1
XM_011515432.2 1092 Missense Mutation CCT,TCT P320S XP_011513734.1
XM_017012361.1 1092 Missense Mutation CCT,TCT P320S XP_016867850.1
XM_017012362.1 1092 UTR 5 XP_016867851.1

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