ClinVar Miner

List of variants in gene ATR reported as benign by GeneDx

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Gene type:
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Total variants: 33
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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.1349+289A>G
NM_001184.4(ATR):c.151+72G>A
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.2805+272T>G
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.4002G>A (p.Gln1334=) rs56026468
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.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.5460T>C (p.Tyr1820=) rs2227932
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.891G>C (p.Lys297Asn) rs2229033

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