List of variants reported as likely benign for Malignant tumor of breast by Center of Medical Genetics and Primary Health Care

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1205G>A (p.Arg402Gln)	rs1126809	0.17677
NM_002386.4(MC1R):c.478C>T (p.Arg160Trp)	rs1805008	0.04620
NM_001365951.3(KIF1B):c.2115+6956A>G	rs148481786	0.00525
NM_001040108.2(MLH3):c.2425A>G (p.Met809Val)	rs61752722	0.00197
NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile)	rs121908162	0.00040
NM_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr)	rs200050883	0.00034
NM_003001.5(SDHC):c.490A>T (p.Met164Leu)	rs200375156	0.00019
NM_001184.4(ATR):c.1411G>C (p.Glu471Gln)	rs371350410	0.00011
NM_000051.4(ATM):c.5890A>G (p.Lys1964Glu)	rs201963507	0.00010
NM_000059.4(BRCA2):c.8359C>T (p.Arg2787Cys)	rs41293517	0.00001

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