List of variants in gene GOT2 studied for epilepsy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002080.4(GOT2):c.1037T>G (p.Val346Gly)	rs30842	0.74625
NM_002080.4(GOT2):c.816C>T (p.Cys272=)	rs1058192	0.71897
NM_002080.4(GOT2):c.228T>G (p.Val76=)	rs14221	0.71031
NM_002080.4(GOT2):c.213T>C (p.Asn71=)	rs257636	0.69895
NM_002080.4(GOT2):c.1009C>G (p.Arg337Gly)	rs1247507359	0.00001
NM_002080.4(GOT2):c.1048C>T (p.Arg350Cys)
NM_002080.4(GOT2):c.1084C>T (p.Leu362Phe)
NM_002080.4(GOT2):c.1097G>T (p.Gly366Val)	rs1597696047
NM_002080.4(GOT2):c.1256G>A (p.Gly419Asp)
NM_002080.4(GOT2):c.233C>T (p.Pro78Leu)
NM_002080.4(GOT2):c.265G>T (p.Ala89Ser)
NM_002080.4(GOT2):c.722T>G (p.Phe241Cys)
NM_002080.4(GOT2):c.784C>G (p.Arg262Gly)	rs752927520
NM_002080.4(GOT2):c.880G>C (p.Val294Leu)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.