Product Details

SNP ID
rs16999100
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:14008485 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTAGTGGTATTTGTCTCACTACAC[A/G]CTTGGCTCATTTTTAGTGGGGGCTA
Phenotype
MIM: 300962
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GEMIN8 PubMed Links

Gene Details

Gene
GEMIN8
Gene Name
gem nuclear organelle associated protein 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042479.1 1500 UTR 3 NP_001035944.1
NM_001042480.1 1500 UTR 3 NP_001035945.1
NM_017856.2 1500 UTR 3 NP_060326.1
XM_005274555.2 1500 Intron XP_005274612.1
XM_017029617.1 1500 Intron XP_016885106.1
XM_017029618.1 1500 Intron XP_016885107.1

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