List of variants in gene KRAS reported as likely pathogenic for B-cell neoplasm

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.182A>T (p.Gln61Leu)	rs121913240
NM_004985.5(KRAS):c.183A>T (p.Gln61His)	rs17851045
NM_033360.4(KRAS):c.351A>C (p.Lys117Asn)	rs770248150
NM_033360.4(KRAS):c.436G>C (p.Ala146Pro)	rs121913527

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