Product Details

SNP ID: rs890793
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.5:154194378 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: TAAGTATAGAAATGTAGCCTTGGAA[C/T]GATTTCCTTAATTTTCCACAGAAGG
Phenotype: MIM: 608043
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: GALNT10 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198321.3		Intron			NP_938080.1