List of variants in gene ATM reported as benign for not provided

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 29

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HGVS	dbSNP
NM_000051.3(ATM):c.1066-6T>G	rs201686625
NM_000051.3(ATM):c.1229T>C (p.Val410Ala)	rs56128736
NM_000051.3(ATM):c.1541G>A (p.Gly514Asp)	rs2235000
NM_000051.3(ATM):c.162T>C (p.Tyr54=)	rs3218690
NM_000051.3(ATM):c.1636C>G (p.Leu546Val)	rs2227924
NM_000051.3(ATM):c.1810C>T (p.Pro604Ser)	rs2227922
NM_000051.3(ATM):c.186-7C>T	rs55674039
NM_000051.3(ATM):c.2119T>C (p.Ser707Pro)	rs4986761
NM_000051.3(ATM):c.2193C>T (p.Tyr731=)	rs2229019
NM_000051.3(ATM):c.2572T>C (p.Phe858Leu)	rs1800056
NM_000051.3(ATM):c.2614C>T (p.Pro872Ser)	rs3218673
NM_000051.3(ATM):c.2685A>G (p.Leu895=)	rs3218687
NM_000051.3(ATM):c.3118A>G (p.Met1040Val)	rs3092857
NM_000051.3(ATM):c.3161C>G (p.Pro1054Arg)	rs1800057
NM_000051.3(ATM):c.3285-9delT	rs1799757
NM_000051.3(ATM):c.3342G>A (p.Lys1114=)	rs138393322
NM_000051.3(ATM):c.3403-15_3403-14insT	rs1555091083
NM_000051.3(ATM):c.378T>A (p.Asp126Glu)	rs2234997
NM_000051.3(ATM):c.4138C>T (p.His1380Tyr)	rs3092856
NM_000051.3(ATM):c.4258C>T (p.Leu1420Phe)	rs1800058
NM_000051.3(ATM):c.4388T>G (p.Phe1463Cys)	rs138327406
NM_000051.3(ATM):c.4473C>T (p.Phe1491=)	rs4988008
NM_000051.3(ATM):c.4980C>T (p.Asn1660=)	rs144338238
NM_000051.3(ATM):c.544G>C (p.Val182Leu)	rs3218707
NM_000051.3(ATM):c.5557G>A (p.Asp1853Asn)	rs1801516
NM_000051.3(ATM):c.5558A>T (p.Asp1853Val)	rs1801673
NM_000051.3(ATM):c.609C>T (p.Asp203=)	rs144709948
NM_000051.3(ATM):c.657T>C (p.Cys219=)	rs2235003
NM_000051.3(ATM):c.735C>T (p.Val245=)	rs3218674

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