Product Details

SNP ID
rs189866517
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:78146437 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTCCCTGGGCTGTTCTGCTTGGC[C/T]GTGCTGGGTGAGTCCACCAGGGACG
Phenotype
MIM: 605829
Polymorphism
C/T, Transition 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_001163075.1 160 Silent Mutation GCC,GCT A10A NP_001156547.1
XM_011524152.2 160 Intron XP_011522454.1
XM_017023997.1 160 Intron XP_016879486.1
XM_017023998.1 160 Silent Mutation GCC,GCT A10A XP_016879487.1
XM_017023999.1 160 Silent Mutation GCC,GCT A10A XP_016879488.1
XM_017024000.1 160 Intron XP_016879489.1
XM_017024001.1 160 Intron XP_016879490.1
Gene
TMC8
Gene Name
transmembrane channel like 8
There are no transcripts associated with this gene.

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