ClinVar Miner

List of variants in gene ATR reported by GeneDx

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Total variants: 76
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HGVS dbSNP
NM_001184.4(ATR):c.-29_-9delinsT rs886058060
NM_001184.4(ATR):c.-6C>T rs769841006
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.2342-20T>C rs983859004
NM_001184.4(ATR):c.2634-74C>T
NM_001184.4(ATR):c.268C>T (p.His90Tyr) rs28897763
NM_001184.4(ATR):c.2704T>C (p.Ser902Pro) rs146202702
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) rs141783863
NM_001184.4(ATR):c.2805+12C>G rs778188323
NM_001184.4(ATR):c.2805+272T>G
NM_001184.4(ATR):c.2844A>C (p.Ala948=) rs147286949
NM_001184.4(ATR):c.289A>T (p.Ile97Phe) rs138473993
NM_001184.4(ATR):c.2958T>C (p.Asp986=) rs143919996
NM_001184.4(ATR):c.2979G>A (p.Arg993=) rs376960547
NM_001184.4(ATR):c.3171+132A>G
NM_001184.4(ATR):c.3171+19A>G rs575077685
NM_001184.4(ATR):c.3171+1G>A rs199731535
NM_001184.4(ATR):c.3241C>T (p.Leu1081=) rs139173669
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly) rs149008479
NM_001184.4(ATR):c.3582-302T>C
NM_001184.4(ATR):c.3642T>C (p.His1214=) rs139078985
NM_001184.4(ATR):c.3726-47A>G rs73240314
NM_001184.4(ATR):c.3945+2dup rs537031994
NM_001184.4(ATR):c.4002G>A (p.Gln1334=) rs56026468
NM_001184.4(ATR):c.4200A>T (p.Leu1400=) rs150562945
NM_001184.4(ATR):c.4266+120A>T
NM_001184.4(ATR):c.4356A>G (p.Glu1452=) rs376297401
NM_001184.4(ATR):c.4376A>G (p.Asn1459Ser) rs144591613
NM_001184.4(ATR):c.437C>A (p.Thr146Lys) rs368592452
NM_001184.4(ATR):c.4383-177C>T
NM_001184.4(ATR):c.4383-19_4383-16del rs768981812
NM_001184.4(ATR):c.4383-232G>T
NM_001184.4(ATR):c.4405A>G (p.Thr1469Ala) rs78895258
NM_001184.4(ATR):c.4503+247A>G
NM_001184.4(ATR):c.4504-263T>A
NM_001184.4(ATR):c.4820G>A (p.Ser1607Asn) rs55724025
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser) rs55894265
NM_001184.4(ATR):c.4852+256T>C
NM_001184.4(ATR):c.5133C>T (p.Ser1711=) rs368178207
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+13A>C rs1553760235
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.5601T>C (p.Leu1867=) rs138891875
NM_001184.4(ATR):c.59+4G>A rs758046042
NM_001184.4(ATR):c.5900G>A (p.Gly1967Asp) rs751198306
NM_001184.4(ATR):c.5931A>G (p.Gln1977=) rs150964938
NM_001184.4(ATR):c.60-20G>T rs1285913916
NM_001184.4(ATR):c.60-51A>T
NM_001184.4(ATR):c.624T>A (p.Thr208=) rs866939836
NM_001184.4(ATR):c.6394T>G (p.Tyr2132Asp) rs28910273
NM_001184.4(ATR):c.6687+262A>G
NM_001184.4(ATR):c.6813A>G (p.Pro2271=) rs774286189
NM_001184.4(ATR):c.6898-15C>T rs1057524789
NM_001184.4(ATR):c.7185A>G (p.Lys2395=) rs749700431
NM_001184.4(ATR):c.7192+18T>C rs1349447137
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.738C>T (p.Ser246=) rs755761580
NM_001184.4(ATR):c.744A>C (p.Ala248=) rs368117837
NM_001184.4(ATR):c.7655+169A>C
NM_001184.4(ATR):c.7667C>G (p.Thr2556Ser) rs200490116
NM_001184.4(ATR):c.7762-174A>G
NM_001184.4(ATR):c.7902C>T (p.Cys2634=)
NM_001184.4(ATR):c.816A>G (p.Ser272=) rs34685245
NM_001184.4(ATR):c.891G>C (p.Lys297Asn) rs2229033
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448

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