Product Details

SNP ID: rs117658637
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:92795772 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATAAAACATGAAGGACTGTGAAGCA[A/G]AAGAATAGGGTATGTACAGATAATG
Phenotype: MIM: 606918
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: GOLGA5 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005113.3		Intron			NP_005104.3
XM_011537420.2		Intron			XP_011535722.1