Product Details

SNP ID
rs114255505
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:81245845 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGCCTCTGGCCCCCCGGGACAGCT[C/G]GTTTGAGCCCCAGCTCTGGCTCTGG
Phenotype
MIM: 616525
Polymorphism
C/G, Transversion 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 2883 Missense Mutation CCA,CGA P1024R NP_001033073.1
NM_138570.3 2883 Intron NP_612637.1
XM_005257019.1 2883 Missense Mutation CCA,CGA P1032R XP_005257076.1
XM_011524288.1 2883 Missense Mutation CCA,CGA P1039R XP_011522590.1
XM_011524289.1 2883 Missense Mutation CCA,CGA P1031R XP_011522591.1
XM_011524290.1 2883 Missense Mutation CCA,CGA P950R 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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