List of variants in gene MAP2K2 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_030662.4(MAP2K2):c.1162C>T (p.Arg388Trp)	rs144383241	0.00222
NM_030662.4(MAP2K2):c.498C>T (p.Pro166=)	rs139404261	0.00076
NM_030662.4(MAP2K2):c.603C>T (p.Leu201=)	rs148291450	0.00072
NM_030662.4(MAP2K2):c.823C>T (p.Leu275=)	rs145934142	0.00070
NM_030662.4(MAP2K2):c.844C>T (p.Pro282Ser)	rs142307980	0.00070
NM_030662.4(MAP2K2):c.1093-6T>C	rs369681843	0.00065
NM_030662.4(MAP2K2):c.1140C>T (p.Ala380=)	rs146618055	0.00034
NM_030662.4(MAP2K2):c.303+12G>A	rs376432107	0.00030
NM_030662.4(MAP2K2):c.525C>T (p.Ile175=)	rs150833333	0.00029
NM_030662.4(MAP2K2):c.678C>T (p.Ser226=)	rs200874968	0.00026
NM_030662.4(MAP2K2):c.1194C>T (p.Thr398=)	rs144850779	0.00024
NM_030662.4(MAP2K2):c.529-12G>A	rs375701469	0.00014
NM_030662.4(MAP2K2):c.784G>A (p.Val262Ile)	rs138873805	0.00014
NM_030662.4(MAP2K2):c.246C>T (p.Asn82=)	rs150942310	0.00013
NM_030662.4(MAP2K2):c.581-8G>A	rs369262004	0.00012
NM_030662.4(MAP2K2):c.*9G>A	rs397517410	0.00009
NM_030662.4(MAP2K2):c.258C>A (p.Val86=)	rs148437150	0.00008
NM_030662.4(MAP2K2):c.939G>T (p.Arg313=)	rs397517417	0.00008
NM_030662.4(MAP2K2):c.281C>T (p.Ser94Leu)	rs202220799	0.00005
NM_030662.4(MAP2K2):c.1065G>A (p.Ala355=)	rs374807671	0.00003
NM_030662.4(MAP2K2):c.705+10C>T	rs372898071	0.00003
NM_030662.4(MAP2K2):c.450+13G>A	rs572847821	0.00002
NM_030662.4(MAP2K2):c.450+14G>A	rs397517414	0.00002
NM_030662.4(MAP2K2):c.474G>A (p.Val158=)	rs370736371	0.00002
NM_030662.4(MAP2K2):c.384G>A (p.Pro128=)	rs727503156	0.00001
NM_030662.4(MAP2K2):c.621G>A (p.Glu207=)	rs397517416	0.00001
NM_030662.4(MAP2K2):c.639C>T (p.Phe213=)	rs727504818	0.00001
NM_030662.4(MAP2K2):c.174C>T (p.Leu58=)	rs876657504
NM_030662.4(MAP2K2):c.564C>T (p.His188=)	rs546749336
NM_030662.4(MAP2K2):c.658A>G (p.Ile220Val)	rs727504363
NM_030662.4(MAP2K2):c.705+11G>A	rs202086678
NM_030662.4(MAP2K2):c.834C>A (p.Ile278=)	rs766540227

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.