Product Details

SNP ID: rs6872685
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:154200232 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGCCGTGCCAGGGCAGGGATTATA[C/G]CAAGTCCCATGTGCCGCCTGGATGC
Phenotype: MIM: 608043
Polymorphism: C/G, Transversion 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