List of variants in gene KRAS reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.407G>A (p.Ser136Asn)	rs757816355	0.00001
NM_004985.5(KRAS):c.487A>G (p.Ile163Val)	rs1470495974	0.00001
NM_033360.4(KRAS):c.389C>T (p.Ala130Val)	rs730880473	0.00001
NM_004985.5(KRAS):c.168C>T (p.Leu56=)	rs958790148
NM_004985.5(KRAS):c.184GAG[1] (p.Glu63del)	rs730880469
NM_004985.5(KRAS):c.331A>G (p.Met111Val)	rs1951384733
NM_004985.5(KRAS):c.352T>C (p.Cys118Arg)	rs1951384485
NM_004985.5(KRAS):c.365C>G (p.Ser122Cys)	rs2141506126
NM_004985.5(KRAS):c.388_389delinsAT (p.Ala130Ile)	rs1951383854
NM_004985.5(KRAS):c.450+5G>A	rs2548918908
NM_004985.5(KRAS):c.451-6T>C
NM_033360.4(KRAS):c.101_106del	rs1339924833

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