ABCDEFGHIJKLMNOPQRSTUVWXYZ
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idvaluemethodcomponent:gene-studiedcomponent:amino-acid-chg
component:variant-consequence
component:functional-effectcomponent:genomic-dna-chgcomponent:sample-allelic-frequencycomponent:allelic-statecomponent:genomic-source-classcomponent:copy-numberextension:SecondaryFindingnotereport
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PTENPresentSequencingPTENp.Y68fsSO:0001589#frameshift_variant;SO:0002054#LOF;SO:0001786#LOHNM_000314:c.203_207del17.80%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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KRASPresentSequencingKRASp.G12DMissense variant (exon 2)SO:0002053#GOFNM_033360:c.35G>A15.80%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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APC1PresentSequencingAPCp.Q1444*SO:0001587#stop gainSO:0002054#LOFNM_000038:c.4330C>T15.50%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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FAT1PresentSequencingFAT1p.E992*SO:0001587#stop gainSO:0002054#LOFNM_005245:c.2974G>T14.90%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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CHEK2PresentSequencingCHEK2p.R145WSO:0001583#Missense variantNM_007194:c.433C>THeterozygousGermlineacmg-version1
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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LMO1PresentSequencingLMO1p.L118ISO:0001583#Missense variantNM_002315:c.352C>A18.20%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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APC2PresentSequencingAPCp.P1439SSO:0001583#Missense variantNM_000038:c.4315C>T14.70%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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LRP1BPresentSequencingLRP1Bp.E3ASO:0001583#Missense variantNM_018557:c.8A>C14.60%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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KAT6APresentSequencingKAT6Ap.M1884ISO:0001583#Missense variantNM_006766:c.5652G>T13.50%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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ATICPresentSequencingATICp.H584NSO:0001583#Missense variantNM_004044:c.1750C>A11.50%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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MAP2K2PresentSequencingMAP2K2p.R313WSO:0001583#Missense variantNM_030662:c.937C>T11.00%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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MYH11PresentSequencingMYH11p.R108WSO:0001583#Missense variantNM_002474:c.322C>T10.10%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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RICTORPresentSequencingRICTORp.K678TSO:0001583#Missense variantNM_001285439:c.2033A>C9.10%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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DPYDPresentSequencingDPYDp.R74QSO:0001583#Missense variantNM_000110:c.221G>A7.60%Somatic
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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BRAFAbsentSequencingBRAF;NRASNo pathogenic single nucleotide variants,
indels, or copy number changes were
found in BRAF
https://drive.google.com/file/d/1wqoVUMP0dDsM4msSrgolv4At7sVDkoN_/view
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EWSR1PresentSequencingEWSR1;ERGSO:0001565#Gene FusionSomatic
https://drive.google.com/file/d/1tbP8mVvMa8WSbMc9nfthf3BZ5-_CEIPz/view
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TP53PresentSequencingTP53p.R196*SO:0001587#stop gainSO:0002054#LOF;SO:0001786#LOHNM_000546:c.586C>T61.40%Somatic
https://drive.google.com/file/d/1tKeoK2DAt3JmLjdcqJfZrd1BvQkROGl1/view
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ARPresentSequencingAR
SO:0001911#Copy number increase
Somatic
https://drive.google.com/file/d/1tKeoK2DAt3JmLjdcqJfZrd1BvQkROGl1/view
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STK11PresentSequencingSTK11
SO:0002084#Exonic splice region variant
SO:0002054#LOFNM_000455:c.465-1G>T38.00%Somatic
https://drive.google.com/file/d/16n9SfVqxvMvQORM_Hz5V7nDt8h2r3vMy/view
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strata1PresentSequencingTP53p.M237INM_000546.5:c.711G>A41%Somatic
https://drive.google.com/file/d/1iFQAFDQ4f182GfyPWCm7mHELiERsfNek/view
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strata2PresentSequencingERBB2
SO:0001880#feature_amplification
Somatic1.9
https://drive.google.com/file/d/1iFQAFDQ4f182GfyPWCm7mHELiERsfNek/view
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