List of variants in gene CHEK2 studied for Breast carcinoma

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1100del (p.Thr367fs)	rs555607708	0.00181
NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_007194.4(CHEK2):c.444+1G>A	rs121908698	0.00009
NM_007194.4(CHEK2):c.342G>A (p.Trp114Ter)	rs756949505	0.00001
NM_007194.4(CHEK2):c.499G>A (p.Gly167Arg)	rs72552322	0.00001
NM_007194.4(CHEK2):c.592+3A>T	rs587782849	0.00001
NM_007194.4(CHEK2):c.58C>T (p.Gln20Ter)	rs536907995
NM_007194.4(CHEK2):c.660_661del (p.Ile221fs)	rs2146005460
NM_007194.4(CHEK2):c.701_720del (p.Val234fs)	rs2145951528
NM_007194.4(CHEK2):c.847-1G>A	rs878854926

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