List of variants in gene RUNX1 reported as likely pathogenic for immune system cancer

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.167T>C (p.Leu56Ser)	rs111527738	0.01206
NM_001754.5(RUNX1):c.1219_1221delinsGGGATCGTTCGGA (p.Tyr407fs)	rs2145875208
NM_001754.5(RUNX1):c.164C>A (p.Ala55Glu)	rs1473182680
NM_001754.5(RUNX1):c.292del (p.Leu98fs)	rs1569084170
NM_001754.5(RUNX1):c.422C>A (p.Ser141Ter)
NM_001754.5(RUNX1):c.484A>G (p.Arg162Gly)	rs1057519751
NM_001754.5(RUNX1):c.485G>A (p.Arg162Lys)	rs1057519750
NM_001754.5(RUNX1):c.486G>C (p.Arg162Ser)	rs1057519749
NM_001754.5(RUNX1):c.486G>T (p.Arg162Ser)	rs1057519749
NM_001754.5(RUNX1):c.508+2T>C	rs1601515707
NM_001754.5(RUNX1):c.601C>T (p.Arg201Ter)	rs1057519748
NM_001754.5(RUNX1):c.777_778dup (p.Asn260fs)
Single allele

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