List of variants in gene KMT2B reported by SIB Swiss Institute of Bioinformatics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_014727.3(KMT2B):c.1633C>T (p.Arg545Ter)	rs1057519279
NM_014727.3(KMT2B):c.1690C>T (p.Arg564Ter)	rs1057519283
NM_014727.3(KMT2B):c.2428C>T (p.Gln810Ter)	rs1057519281
NM_014727.3(KMT2B):c.4545C>A (p.Tyr1515Ter)	rs1057519284
NM_014727.3(KMT2B):c.4955G>A (p.Gly1652Asp)	rs1555731832
NM_014727.3(KMT2B):c.4986C>A (p.Phe1662Leu)	rs372432644
NM_014727.3(KMT2B):c.5114G>A (p.Arg1705Gln)	rs1555731980
NM_014727.3(KMT2B):c.5284C>T (p.Arg1762Cys)	rs1489232377
NM_014727.3(KMT2B):c.5342T>C (p.Leu1781Pro)	rs1555732094
NM_014727.3(KMT2B):c.7549C>T (p.Arg2517Trp)	rs1057519285
NM_014727.3(KMT2B):c.8021T>C (p.Ile2674Thr)	rs1555735051

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