ClinVar Miner

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

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Total variants: 41
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HGVS dbSNP
NM_001184.4(ATR):c.1170+148_1170+149insA
NM_001184.4(ATR):c.1170+150_1170+151insA
NM_001184.4(ATR):c.1326A>G (p.Lys442=) rs28897765
NM_001184.4(ATR):c.1349+289A>G
NM_001184.4(ATR):c.151+72G>A
NM_001184.4(ATR):c.1776T>A (p.Gly592=) rs2227930
NM_001184.4(ATR):c.1950G>A (p.Glu650=) rs28910270
NM_001184.4(ATR):c.2341+185G>A
NM_001184.4(ATR):c.2342-175A>G
NM_001184.4(ATR):c.2634-74C>T
NM_001184.4(ATR):c.268C>T (p.His90Tyr) rs28897763
NM_001184.4(ATR):c.2805+272T>G
NM_001184.4(ATR):c.2875G>A (p.Val959Met) rs28910271
NM_001184.4(ATR):c.293-20C>T rs115097590
NM_001184.4(ATR):c.3120G>A (p.Leu1040=) rs28910272
NM_001184.4(ATR):c.3171+132A>G
NM_001184.4(ATR):c.3582-302T>C
NM_001184.4(ATR):c.3726-47A>G rs73240314
NM_001184.4(ATR):c.4153-10del rs112116713
NM_001184.4(ATR):c.4153-21dup rs112116713
NM_001184.4(ATR):c.4266+120A>T
NM_001184.4(ATR):c.4383-177C>T
NM_001184.4(ATR):c.4383-232G>T
NM_001184.4(ATR):c.4503+247A>G
NM_001184.4(ATR):c.4504-263T>A
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser) rs55894265
NM_001184.4(ATR):c.4852+256T>C
NM_001184.4(ATR):c.5196+109G>A
NM_001184.4(ATR):c.5197-289A>G
NM_001184.4(ATR):c.5208T>C (p.Tyr1736=) rs2227931
NM_001184.4(ATR):c.5288+130G>A
NM_001184.4(ATR):c.5288+248T>C
NM_001184.4(ATR):c.5380+121C>A
NM_001184.4(ATR):c.5381-41C>T rs34502778
NM_001184.4(ATR):c.60-51A>T
NM_001184.4(ATR):c.6687+262A>G
NM_001184.4(ATR):c.7274G>A (p.Arg2425Gln) rs2229032
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala) rs33972295
NM_001184.4(ATR):c.7655+169A>C
NM_001184.4(ATR):c.7762-174A>G
NM_001184.4(ATR):c.7875G>A (p.Gln2625=) rs1802904

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