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Variants search result for Homo sapiens
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70 records found for search term Ascc2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156282033CV2220693single nucleotide variantNM_032204.5(ASCC2):c.77C>T (p.Ala26Val)not specified [RCV004097867]uncertain significance222983224929832249Humanname
401741789CV2710275single nucleotide variantNM_032204.5(ASCC2):c.92A>G (p.Gln31Arg)not specified [RCV004317167]uncertain significance222982577029825770Humanname
156138113CV2280638single nucleotide variantNM_032204.5(ASCC2):c.253G>A (p.Glu85Lys)not specified [RCV004143112]uncertain significance222982524529825245Humanname
156053198CV2312429single nucleotide variantNM_032204.5(ASCC2):c.173G>A (p.Arg58His)not specified [RCV004167115]uncertain significance222982568929825689Humanname
155968012CV2312784single nucleotide variantNM_032204.5(ASCC2):c.289T>C (p.Tyr97His)not specified [RCV004169498]uncertain significance222982520929825209Humanname
405675851CV3286832single nucleotide variantNM_032204.5(ASCC2):c.148G>A (p.Ala50Thr)not specified [RCV004420640]uncertain significance222982571429825714Humanname
597786051CV3594363single nucleotide variantNM_032204.5(ASCC2):c.133A>G (p.Lys45Glu)not specified [RCV004854905]uncertain significance222982572929825729Humanname
598190985CV3902829single nucleotide variantNM_032204.5(ASCC2):c.278C>T (p.Ser93Phe)not specified [RCV005266924]uncertain significance222982522029825220Humanname
598191138CV3902849single nucleotide variantNM_032204.5(ASCC2):c.109T>G (p.Phe37Val)not specified [RCV005266944]uncertain significance222982575329825753Humanname
156186951CV2232715single nucleotide variantNM_032204.5(ASCC2):c.598A>G (p.Thr200Ala)not specified [RCV004101373]uncertain significance222981601729816017Humanname
156138725CV2250301single nucleotide variantNM_032204.5(ASCC2):c.729G>C (p.Lys243Asn)not specified [RCV004127199]uncertain significance222981353429813534Humanname
329388424CV2471921single nucleotide variantNM_032204.5(ASCC2):c.745C>G (p.Leu249Val)not specified [RCV004280942]uncertain significance222981351829813518Humanname
401757567CV2675379single nucleotide variantNM_032204.5(ASCC2):c.613T>C (p.Phe205Leu)not specified [RCV004292186]uncertain significance222981476429814764Humanname
401719937CV2705580single nucleotide variantNM_032204.5(ASCC2):c.865G>A (p.Glu289Lys)not specified [RCV004318444]uncertain significance222980815429808154Humanname
401772496CV2719659single nucleotide variantNM_032204.5(ASCC2):c.514A>G (p.Asn172Asp)not specified [RCV004327321]uncertain significance222982236229822362Humanname
405675919CV3286845single nucleotide variantNM_032204.5(ASCC2):c.707A>G (p.Asp236Gly)not specified [RCV004420653]uncertain significance222981467029814670Humanname
405675925CV3286846single nucleotide variantNM_032204.5(ASCC2):c.739C>G (p.Leu247Val)not specified [RCV004420654]uncertain significance222981352429813524Humanname
405675930CV3286847single nucleotide variantNM_032204.5(ASCC2):c.917G>T (p.Gly306Val)not specified [RCV004420655]uncertain significance222980689629806896Humanname
407489581CV3473807single nucleotide variantNM_032204.5(ASCC2):c.362G>A (p.Arg121Gln)not specified [RCV004666085]uncertain significance222982513629825136Humanname
597786032CV3594353single nucleotide variantNM_032204.5(ASCC2):c.769T>G (p.Trp257Gly)not specified [RCV004854901]uncertain significance222981349429813494Humanname
598191199CV3902858single nucleotide variantNM_032204.5(ASCC2):c.658A>G (p.Asn220Asp)not specified [RCV005266953]uncertain significance222981471929814719Humanname
156233543CV2197128single nucleotide variantNM_032204.5(ASCC2):c.1042G>A (p.Glu348Lys)not specified [RCV004071556]uncertain significance222980652829806528Humanname
156189372CV2205932single nucleotide variantNM_032204.5(ASCC2):c.1916G>T (p.Arg639Leu)not specified [RCV004078363]uncertain significance222979336329793363Humanname
156079869CV2226579single nucleotide variantNM_032204.5(ASCC2):c.2078G>A (p.Arg693His)not specified [RCV004101833]uncertain significance222979049329790493Humanname
156362837CV2265616single nucleotide variantNM_032204.5(ASCC2):c.2144G>A (p.Arg715Gln)not specified [RCV004124348]uncertain significance222978914329789143Humanname
156336385CV2270714single nucleotide variantNM_032204.5(ASCC2):c.1928C>T (p.Thr643Ile)not specified [RCV004131781]uncertain significance222979252729792527Humanname
156258071CV2322113single nucleotide variantNM_032204.5(ASCC2):c.1909A>T (p.Ile637Phe)not specified [RCV004173854]uncertain significance222979337029793370Humanname
156278238CV2328438single nucleotide variantNM_032204.5(ASCC2):c.1261G>A (p.Glu421Lys)not specified [RCV004175538]uncertain significance222980473029804730Humanname
156078758CV2341210single nucleotide variantNM_032204.5(ASCC2):c.1292C>T (p.Thr431Met)not specified [RCV004186627]uncertain significance222980469929804699Humanname
155923051CV2347432single nucleotide variantNM_032204.5(ASCC2):c.1559A>G (p.Asn520Ser)not specified [RCV004207266]likely benign222980200329802003Humanname
156237775CV2356207single nucleotide variantNM_032204.5(ASCC2):c.1525C>T (p.Arg509Trp)not specified [RCV004206026]uncertain significance222980203729802037Humanname
155928511CV2360053single nucleotide variantNM_032204.5(ASCC2):c.1556G>A (p.Arg519His)not specified [RCV004212886]uncertain significance222980200629802006Humanname
156254092CV2366381single nucleotide variantNM_032204.5(ASCC2):c.2177A>G (p.Glu726Gly)not specified [RCV004212432]uncertain significance222978911029789110Humanname
155937534CV2380034single nucleotide variantNM_032204.5(ASCC2):c.1730A>G (p.Lys577Arg)not specified [RCV004222170]uncertain significance222979363529793635Humanname
329360923CV2463113single nucleotide variantNM_032204.5(ASCC2):c.1220A>C (p.Asp407Ala)not specified [RCV004274913]uncertain significance222980477129804771Humanname
401774143CV2691532single nucleotide variantNM_032204.5(ASCC2):c.1073T>C (p.Leu358Pro)not specified [RCV004305368]uncertain significance222980649729806497Humanname
401762346CV2696095single nucleotide variantNM_032204.5(ASCC2):c.1334A>G (p.Glu445Gly)not specified [RCV004310158]uncertain significance222980465729804657Humanname
401865313CV2754218single nucleotide variantNM_032204.5(ASCC2):c.1873G>A (p.Val625Met)not specified [RCV004334407]uncertain significance222979340629793406Humanname
401855812CV2757483single nucleotide variantNM_032204.5(ASCC2):c.1585C>T (p.Pro529Ser)not specified [RCV004340870]uncertain significance222980109429801094Humanname
405675813CV3286825single nucleotide variantNM_032204.5(ASCC2):c.1132A>G (p.Ser378Gly)not specified [RCV004420633]uncertain significance222980624429806244Humanname
405675818CV3286826single nucleotide variantNM_032204.5(ASCC2):c.1132A>T (p.Ser378Cys)not specified [RCV004420634]uncertain significance222980624429806244Humanname
405675824CV3286827single nucleotide variantNM_032204.5(ASCC2):c.1216G>A (p.Val406Met)not specified [RCV004420635]uncertain significance222980477529804775Humanname
405675830CV3286828single nucleotide variantNM_032204.5(ASCC2):c.1337A>T (p.Asn446Ile)not specified [RCV004420636]uncertain significance222980465429804654Humanname
405675835CV3286829single nucleotide variantNM_032204.5(ASCC2):c.1389G>A (p.Met463Ile)not specified [RCV004420637]uncertain significance222980217329802173Humanname
405675841CV3286830single nucleotide variantNM_032204.5(ASCC2):c.1441G>T (p.Asp481Tyr)not specified [RCV004420638]uncertain significance222980212129802121Humanname
405675846CV3286831single nucleotide variantNM_032204.5(ASCC2):c.1487A>G (p.Tyr496Cys)not specified [RCV004420639]uncertain significance222980207529802075Humanname
405675855CV3286833single nucleotide variantNM_032204.5(ASCC2):c.1554C>A (p.Asp518Glu)not specified [RCV004420641]uncertain significance222980200829802008Humanname
405675861CV3286834single nucleotide variantNM_032204.5(ASCC2):c.1669C>T (p.Arg557Trp)not specified [RCV004420642]uncertain significance222980101029801010Humanname
405676394CV3286835single nucleotide variantNM_032204.5(ASCC2):c.1685A>G (p.Lys562Arg)not specified [RCV004420643]likely benign222980099429800994Humanname
405675870CV3286836single nucleotide variantNM_032204.5(ASCC2):c.1757G>T (p.Arg586Leu)not specified [RCV004420644]uncertain significance222979360829793608Humanname
405675876CV3286837single nucleotide variantNM_032204.5(ASCC2):c.1812C>G (p.Ser604Arg)not specified [RCV004420645]uncertain significance222979346729793467Humanname
405675881CV3286838single nucleotide variantNM_032204.5(ASCC2):c.1915C>A (p.Arg639Ser)not specified [RCV004420646]uncertain significance222979336429793364Humanname
405675893CV3286840single nucleotide variantNM_032204.5(ASCC2):c.2008G>A (p.Glu670Lys)not specified [RCV004420648]uncertain significance222979244729792447Humanname
405675898CV3286841single nucleotide variantNM_032204.5(ASCC2):c.2020A>C (p.Lys674Gln)not specified [RCV004420649]uncertain significance222979243529792435Humanname
405675903CV3286842single nucleotide variantNM_032204.5(ASCC2):c.2162G>A (p.Arg721His)not specified [RCV004420650]uncertain significance222978912529789125Humanname
405675909CV3286843single nucleotide variantNM_032204.5(ASCC2):c.2204C>T (p.Ala735Val)not specified [RCV004420651]uncertain significance222978908329789083Humanname
405675914CV3286844single nucleotide variantNM_032204.5(ASCC2):c.2225G>A (p.Arg742Gln)not specified [RCV004420652]uncertain significance222978906229789062Humanname
407489612CV3483894single nucleotide variantNM_032204.5(ASCC2):c.1108C>T (p.Leu370Phe)not specified [RCV004666093]uncertain significance222980626829806268Humanname
597785893CV3594296single nucleotide variantNM_032204.5(ASCC2):c.2213C>G (p.Ala738Gly)not specified [RCV004854867]uncertain significance222978907429789074Humanname
597785916CV3594305single nucleotide variantNM_032204.5(ASCC2):c.1606C>T (p.Arg536Cys)not specified [RCV004854872]uncertain significance222980107329801073Humanname
597785952CV3594315single nucleotide variantNM_032204.5(ASCC2):c.1210G>A (p.Glu404Lys)not specified [RCV004854880]uncertain significance222980478129804781Humanname
597785978CV3594326single nucleotide variantNM_032204.5(ASCC2):c.2180G>C (p.Arg727Pro)not specified [RCV004854887]uncertain significance222978910729789107Humanname
597709835CV3594337single nucleotide variantNM_032204.5(ASCC2):c.1139T>C (p.Leu380Pro)not specified [RCV004860886]uncertain significance222980623729806237Humanname
597709887CV3594345single nucleotide variantNM_032204.5(ASCC2):c.1861G>C (p.Asp621His)not specified [RCV004860892]uncertain significance222979341829793418Humanname
598190632CV3902781single nucleotide variantNM_032204.5(ASCC2):c.1240G>T (p.Ala414Ser)not specified [RCV005266876]uncertain significance222980475129804751Humanname
598190683CV3902788single nucleotide variantNM_032204.5(ASCC2):c.1681G>A (p.Gly561Ser)not specified [RCV005266883]uncertain significance222980099829800998Humanname
598190754CV3902798single nucleotide variantNM_032204.5(ASCC2):c.1555C>T (p.Arg519Cys)not specified [RCV005266893]uncertain significance222980200729802007Humanname
598190832CV3902809single nucleotide variantNM_032204.5(ASCC2):c.1916G>A (p.Arg639His)not specified [RCV005266904]uncertain significance222979336329793363Humanname
598190897CV3902818single nucleotide variantNM_032204.5(ASCC2):c.1690A>G (p.Thr564Ala)not specified [RCV005266913]likely benign222979367529793675Humanname
598191062CV3902840single nucleotide variantNM_032204.5(ASCC2):c.1699G>A (p.Glu567Lys)not specified [RCV005266935]uncertain significance222979366629793666Humanname