Product Details

SNP ID
rs189910554
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:30744190 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTGCACCAGGCGCTTCCGCCACC[A/G]TGGCTTCACGTGGGGTTGTTGGCAT
Phenotype
MIM: 602155
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC105379356 PubMed Links

Gene Details

Gene
LOC105379356
Gene Name
uncharacterized LOC105379356
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_017014155.1 26 Intron XP_016869644.1
XM_017014156.1 26 Intron XP_016869645.1
Gene
UBXN8
Gene Name
UBX domain protein 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282189.1 26 Missense Mutation ATG,GTG M1V NP_001269118.1
NM_001282199.1 26 Missense Mutation ATG,GTG M1V NP_001269128.1
NM_005671.3 26 Missense Mutation ATG,GTG M1V NP_005662.1
XM_011544655.2 26 Intron XP_011542957.1
XM_017013862.1 26 Intron XP_016869351.1

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