Product Details

SNP ID
rs144652569
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:111691831 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTCTGAGAGTACAATTTGTTACA[C/T]GCAGTCTGCTGTGCACCATATTGTA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C9orf84 PubMed Links

Gene Details

Gene
C9orf84
Gene Name
chromosome 9 open reading frame 84
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080551.2 4275 Silent Mutation GCA,GCG A1279A NP_001074020.2
NM_173521.4 4275 Silent Mutation GCA,GCG A1318A NP_775792.4
XM_006716974.2 4275 Silent Mutation GCA,GCG A1382A XP_006717037.1
XM_006716975.2 4275 Silent Mutation GCA,GCG A1347A XP_006717038.1
XM_011518302.2 4275 Silent Mutation GCA,GCG A1318A XP_011516604.1
XM_011518303.1 4275 Silent Mutation GCA,GCG A1318A XP_011516605.1
XM_011518306.1 4275 Silent Mutation GCA,GCG A1193A XP_011516608.1
XM_011518309.1 4275 Intron XP_011516611.1
XM_017014340.1 4275 Silent Mutation GCA,GCG A1269A XP_016869829.1
XM_017014341.1 4275 Intron XP_016869830.1

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