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SNP ID: rs201073991
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:31490360 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTCCGCCAGTGCCTGCTCTGGTTTT[C/G]TGGAATGAGCAGAGGTGGGGTGGGC
Phenotype: MIM: 182381
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: C16orf58 PubMed Links

Gene Details

Gene: C16orf58
Gene Name: chromosome 16 open reading frame 58

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022744.3	1759	UTR 3			NP_073581.2
XM_017023570.1	1759	UTR 3			XP_016879059.1

Gene: LOC105371171
Gene Name: uncharacterized LOC105371171

There are no transcripts associated with this gene.

Gene: SLC5A2
Gene Name: solute carrier family 5 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003041.3	1759	Missense Mutation	TCT,TGT	S615C	NP_003032.1
XM_006721072.3	1759	Missense Mutation	TCT,TGT	S648C	XP_006721135.2

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