ClinVar Miner

List of variants in gene KMT2C reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_170606.3(KMT2C):c.12817C>T (p.Pro4273Ser) rs145997023 0.00036
NM_170606.3(KMT2C):c.14534+17C>T rs199939483 0.00005
NM_170606.3(KMT2C):c.11341T>C (p.Leu3781=) rs571360111 0.00003
NM_170606.3(KMT2C):c.14534+15A>T rs373983978 0.00002
NM_170606.3(KMT2C):c.14410A>G (p.Ile4804Val) rs760982267 0.00001
NM_170606.3(KMT2C):c.1458T>C (p.Asn486=) rs1482178225 0.00001
NM_170606.3(KMT2C):c.3324-19A>C rs762040193 0.00001
NM_170606.3(KMT2C):c.5580C>T (p.Ser1860=) rs776101090 0.00001
NC_000007.13:g.(?_151832009)_(152055761_152132710)dup
NM_170606.3(KMT2C):c.10716A>G (p.Gln3572=)
NM_170606.3(KMT2C):c.14343+9A>G rs1422109550
NM_170606.3(KMT2C):c.250+16A>G rs2097171010
NM_170606.3(KMT2C):c.3792G>A (p.Val1264=)
NM_170606.3(KMT2C):c.5343G>A (p.Gln1781=) rs1225974576
NM_170606.3(KMT2C):c.6330C>T (p.Ala2110=)
NM_170606.3(KMT2C):c.6339A>C (p.Ser2113=) rs73161892
NM_170606.3(KMT2C):c.7086A>C (p.Ser2362=) rs149651977
NM_170606.3(KMT2C):c.7402C>T (p.Pro2468Ser)
NM_170606.3(KMT2C):c.7953T>C (p.His2651=)
NM_170606.3(KMT2C):c.8919G>T (p.Val2973=) rs780725159
NM_170606.3(KMT2C):c.8991A>G (p.Gln2997=)

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.