Product Details

SNP ID
rs75472704
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:81245902 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGGCTCCTGGACAGCAGCGTCC[C/T]CCCCGCCTCTCGGCTGCTCGTGGGA
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 2826 Missense Mutation GAG,GGG E1005G NP_001033073.1
NM_138570.3 2826 Intron NP_612637.1
XM_005257019.1 2826 Missense Mutation GAG,GGG E1013G XP_005257076.1
XM_011524288.1 2826 Missense Mutation GAG,GGG E1020G XP_011522590.1
XM_011524289.1 2826 Missense Mutation GAG,GGG E1012G XP_011522591.1
XM_011524290.1 2826 Missense Mutation GAG,GGG E931G 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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