Product Details

SNP ID
rs61740863
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:81246216 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTCAGAATGCTGGTGCCAGTGGC[C/T]GCCACCTCCTTCCCAGGTTTTTTCC
Phenotype
MIM: 616525
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C17orf89 PubMed Links

Gene Details

Gene
C17orf89
Gene Name
chromosome 17 open reading frame 89
There are no transcripts associated with this gene.

Gene
SLC38A10
Gene Name
solute carrier family 38 member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037984.2 2512 Silent Mutation GCC,GCT A900A NP_001033073.1
NM_138570.3 2512 Intron NP_612637.1
XM_005257019.1 2512 Silent Mutation GCC,GCT A908A XP_005257076.1
XM_011524288.1 2512 Silent Mutation GCC,GCT A915A XP_011522590.1
XM_011524289.1 2512 Silent Mutation GCC,GCT A907A XP_011522591.1
XM_011524290.1 2512 Silent Mutation GCC,GCT A826A XP_011522592.1
Gene
TEPSIN
Gene Name
TEPSIN, adaptor related protein complex 4 accessory protein
There are no transcripts associated with this gene.

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