Product Details

SNP ID
rs4789016
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:78156926 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCGTGCCTGGACACATTTTGTTT[A/T]TATAGAAAAATATTCTGGAAAGAAA
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
C17orf99 PubMed Links

Gene Details

Gene
C17orf99
Gene Name
chromosome 17 open reading frame 99
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001163075.1 172 Intron NP_001156547.1
XM_011524152.2 172 Intron XP_011522454.1
XM_017023997.1 172 Intron XP_016879486.1
XM_017023998.1 172 Intron XP_016879487.1
XM_017023999.1 172 Intron XP_016879488.1
XM_017024000.1 172 UTR 5 XP_016879489.1
XM_017024001.1 172 Intron XP_016879490.1

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