Product Details

SNP ID
rs199743843
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:7572839 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGACAATGTAATACCCTTGCCTGG[A/C]ATCCACTGGATAGTAACTGGCTAGC
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_019005.3 498 Missense Mutation AAT,CAT N122H NP_061878.3
XM_005249780.3 498 Missense Mutation AAT,CAT N122H XP_005249837.1
XM_005249781.3 498 Missense Mutation AAT,CAT N122H XP_005249838.1
XM_005249782.3 498 Missense Mutation AAT,CAT N122H XP_005249839.1
XM_005249784.3 498 Missense Mutation AAT,CAT N122H XP_005249841.1
XM_011515432.2 498 Missense Mutation AAT,CAT N122H XP_011513734.1
XM_017012361.1 498 Missense Mutation AAT,CAT N122H XP_016867850.1
XM_017012362.1 498 UTR 5 XP_016867851.1

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