Product Details

SNP ID
rs147264354
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:69631751 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCACAGCGCCTGGGAGGATGGTGC[A/G]GATCTTGGCCAATGGGGAAATCGTG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C10orf35 PubMed Links

Gene Details

Gene
C10orf35
Gene Name
chromosome 10 open reading frame 35
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145306.2 719 Missense Mutation CAG,CGG Q3R NP_660349.1
XM_005269606.1 719 Missense Mutation CAG,CGG Q45R XP_005269663.1
XM_005269608.3 719 Missense Mutation CAG,CGG Q3R XP_005269665.1
XM_011539455.2 719 Missense Mutation CAG,CGG Q3R XP_011537757.1
XM_017015836.1 719 Missense Mutation CAG,CGG Q3R XP_016871325.1

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