ClinVar Miner

List of variants in gene MAP2K2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_030662.4(MAP2K2):c.1191C>T (p.Arg397=) rs148592592 0.00031
NM_030662.4(MAP2K2):c.784G>A (p.Val262Ile) rs138873805 0.00014
NM_030662.4(MAP2K2):c.399C>T (p.Phe133=) rs145524962 0.00008
NM_030662.4(MAP2K2):c.853G>A (p.Asp285Asn) rs150369301 0.00008
NM_030662.4(MAP2K2):c.1112G>A (p.Arg371Gln) rs730880514 0.00006
NM_030662.4(MAP2K2):c.1187C>T (p.Thr396Met) rs117945277 0.00004
NM_030662.4(MAP2K2):c.274A>G (p.Arg92Gly) rs759061964 0.00004
NM_030662.4(MAP2K2):c.648C>T (p.Ser216=) rs147276536 0.00004
NM_030662.4(MAP2K2):c.889C>T (p.Arg297Trp) rs562352756 0.00004
NM_030662.4(MAP2K2):c.93-6C>T rs727504836 0.00004
NM_030662.4(MAP2K2):c.1065G>A (p.Ala355=) rs374807671 0.00003
NM_030662.4(MAP2K2):c.1176C>T (p.Pro392=) rs529064753 0.00003
NM_030662.4(MAP2K2):c.1182A>G (p.Thr394=) rs375253105 0.00003
NM_030662.4(MAP2K2):c.477G>A (p.Leu159=) rs748135585 0.00003
NM_030662.4(MAP2K2):c.818A>G (p.Lys273Arg) rs539555837 0.00003
NM_030662.4(MAP2K2):c.1197C>T (p.Ala399=) rs987393686 0.00002
NM_030662.4(MAP2K2):c.474G>A (p.Val158=) rs370736371 0.00002
NM_030662.4(MAP2K2):c.1092A>G (p.Thr364=) rs779378237 0.00001
NM_030662.4(MAP2K2):c.207C>T (p.Asp69=) rs199850535 0.00001
NM_030662.4(MAP2K2):c.357G>A (p.Leu119=) rs1377039329 0.00001
NM_030662.4(MAP2K2):c.384G>A (p.Pro128=) rs727503156 0.00001
NM_030662.4(MAP2K2):c.390C>T (p.Ile130=) rs749956316 0.00001
NM_030662.4(MAP2K2):c.639C>T (p.Phe213=) rs727504818 0.00001
NM_030662.4(MAP2K2):c.699C>T (p.Tyr233=) rs1044588100 0.00001
NM_030662.4(MAP2K2):c.990T>A (p.Pro330=) rs1454910757 0.00001
NM_030662.4(MAP2K2):c.1080G>A (p.Leu360=) rs2040885847
NM_030662.4(MAP2K2):c.750C>T (p.Ile250=) rs2040968148
NM_030662.4(MAP2K2):c.813C>G (p.Asp271Glu) rs201726622
NM_030662.4(MAP2K2):c.847G>A (p.Val283Met) rs185999703
NM_030662.4(MAP2K2):c.860AAG[1] (p.Glu288del) rs763469132
NM_030662.4(MAP2K2):c.985-14G>C

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.