Product Details

SNP ID
rs9906439
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:78151739 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGAGAGAGGGGGAGCCATCTGTAAA[A/T]ACCTGATTTCCAAATATGTTCCCAT
Phenotype
MIM: 605829
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 Intron NP_001156547.1
XM_011524152.2 Intron XP_011522454.1
XM_017023997.1 Intron XP_016879486.1
XM_017023998.1 Intron XP_016879487.1
XM_017023999.1 Intron XP_016879488.1
XM_017024000.1 Intron XP_016879489.1
XM_017024001.1 Intron XP_016879490.1
Gene
TMC8
Gene Name
transmembrane channel like 8
There are no transcripts associated with this gene.

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