Product Details

SNP ID: rs75356568
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:38213138 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGAAGCTGCCCCCAGTGAGGCGAGG[A/G]ACCTGGCTCTGCCTGGGGGGCTGCT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: KIAA1755 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001029864.1	3779	Silent Mutation	GTC,GTT	V1169V	NP_001025035.1