ClinVar Miner

List of variants in gene combination CBR4, PALLD reported as likely benign for adenocarcinoma

Included ClinVar conditions (108):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 107
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.33-4G>A rs113515140 0.00105
NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr) rs142116575 0.00102
NM_001166108.2(PALLD):c.2976G>A (p.Thr992=) rs143717202 0.00033
NM_001166108.2(PALLD):c.2101-9G>A rs368890611 0.00019
NM_001166108.2(PALLD):c.2723G>A (p.Arg908His) rs114171764 0.00011
NM_001166108.2(PALLD):c.3087T>A (p.Phe1029Leu) rs189021816 0.00010
NM_001166108.2(PALLD):c.3321A>G (p.Ala1107=) rs764265611 0.00010
NM_001166108.2(PALLD):c.3351C>T (p.Asp1117=) rs115937217 0.00010
NM_001166108.2(PALLD):c.2975C>T (p.Thr992Met) rs750033888 0.00009
NM_001166108.2(PALLD):c.2473-4A>G rs765144938 0.00004
NM_001166108.2(PALLD):c.2901C>T (p.Pro967=) rs533269596 0.00004
NM_001166108.2(PALLD):c.3224+14A>G rs766796340 0.00003
NM_001166108.2(PALLD):c.3358+9C>G rs746599370 0.00003
NM_001166108.2(PALLD):c.*109G>A rs1002500543 0.00002
NM_001166108.2(PALLD):c.*124C>T rs369747738 0.00002
NM_001166108.2(PALLD):c.2101-10C>T rs757885388 0.00002
NM_001166108.2(PALLD):c.2130T>C (p.Arg710=) rs749041581 0.00002
NM_001166108.2(PALLD):c.2850+15T>C rs977479187 0.00002
NM_001166108.2(PALLD):c.2961C>T (p.Ile987=) rs1484758238 0.00002
NM_001166108.2(PALLD):c.2988C>T (p.Ala996=) rs748161189 0.00002
NM_001166108.2(PALLD):c.3243C>T (p.His1081=) rs779615947 0.00002
NM_001166108.2(PALLD):c.*100A>G rs754444061 0.00001
NM_001166108.2(PALLD):c.*163C>T rs777453756 0.00001
NM_001166108.2(PALLD):c.*187A>G rs1177108180 0.00001
NM_001166108.2(PALLD):c.*196G>A rs896702235 0.00001
NM_001166108.2(PALLD):c.*67A>G rs1424841441 0.00001
NM_001166108.2(PALLD):c.2112C>T (p.Tyr704=) rs372414187 0.00001
NM_001166108.2(PALLD):c.2133A>G (p.Arg711=) rs374250410 0.00001
NM_001166108.2(PALLD):c.2148C>T (p.Asp716=) rs1335231320 0.00001
NM_001166108.2(PALLD):c.2175G>A (p.Glu725=) rs762267147 0.00001
NM_001166108.2(PALLD):c.2268C>T (p.Ser756=) rs931772731 0.00001
NM_001166108.2(PALLD):c.2304G>A (p.Arg768=) rs748432333 0.00001
NM_001166108.2(PALLD):c.2382A>G (p.Pro794=) rs757114919 0.00001
NM_001166108.2(PALLD):c.2517T>C (p.Asp839=) rs934779804 0.00001
NM_001166108.2(PALLD):c.2532A>G (p.Gln844=) rs754158038 0.00001
NM_001166108.2(PALLD):c.2622+9G>A rs769517051 0.00001
NM_001166108.2(PALLD):c.2688G>T (p.Arg896=) rs1257537496 0.00001
NM_001166108.2(PALLD):c.2745A>G (p.Gly915=) rs200328911 0.00001
NM_001166108.2(PALLD):c.2862A>G (p.Leu954=) rs1306143762 0.00001
NM_001166108.2(PALLD):c.2904A>G (p.Val968=) rs781313666 0.00001
NM_001166108.2(PALLD):c.2922C>T (p.His974=) rs1445122482 0.00001
NM_001166108.2(PALLD):c.3066A>G (p.Glu1022=) rs773814059 0.00001
NM_001166108.2(PALLD):c.3177T>C (p.Phe1059=) rs778134231 0.00001
NM_001166108.2(PALLD):c.3258G>A (p.Leu1086=) rs150256686 0.00001
NM_001166108.2(PALLD):c.3358+7_3358+8dup rs1560937938 0.00001
NM_001166108.2(PALLD):c.*112C>T
NM_001166108.2(PALLD):c.*136G>A rs752296365
NM_001166108.2(PALLD):c.*136G>C
NM_001166108.2(PALLD):c.*136G>T
NM_001166108.2(PALLD):c.*172G>A rs1762578631
NM_001166108.2(PALLD):c.*33-14C>G rs2126616657
NM_001166108.2(PALLD):c.*33-8C>T
NM_001166108.2(PALLD):c.*43T>C rs796831946
NM_001166108.2(PALLD):c.2101-11_2101-10del rs2151217010
NM_001166108.2(PALLD):c.2101-11dup
NM_001166108.2(PALLD):c.2101-20T>G
NM_001166108.2(PALLD):c.2101-6_2101-4del rs867266337
NM_001166108.2(PALLD):c.2169T>A (p.Ile723=) rs2151217538
NM_001166108.2(PALLD):c.2199+16G>A
NM_001166108.2(PALLD):c.2199+18A>G
NM_001166108.2(PALLD):c.2251-12T>C
NM_001166108.2(PALLD):c.2274A>G (p.Glu758=)
NM_001166108.2(PALLD):c.2298G>A (p.Glu766=)
NM_001166108.2(PALLD):c.2319T>C (p.Pro773=) rs961514057
NM_001166108.2(PALLD):c.2370T>C (p.Asn790=)
NM_001166108.2(PALLD):c.2442A>C (p.Thr814=)
NM_001166108.2(PALLD):c.2466G>A (p.Lys822=) rs2151264658
NM_001166108.2(PALLD):c.2472+8G>A
NM_001166108.2(PALLD):c.2473-10C>G
NM_001166108.2(PALLD):c.2473-18C>T
NM_001166108.2(PALLD):c.2541C>G (p.Leu847=)
NM_001166108.2(PALLD):c.2541C>T (p.Leu847=) rs863224382
NM_001166108.2(PALLD):c.2550C>G (p.Thr850=) rs772737020
NM_001166108.2(PALLD):c.2586T>C (p.Asp862=) rs1431878477
NM_001166108.2(PALLD):c.2598T>C (p.Tyr866=) rs997146277
NM_001166108.2(PALLD):c.2622+8A>G rs2151306705
NM_001166108.2(PALLD):c.2623-8T>C rs2151407394
NM_001166108.2(PALLD):c.2625C>T (p.Gly875=) rs2151407453
NM_001166108.2(PALLD):c.2814T>A (p.Thr938=)
NM_001166108.2(PALLD):c.2850+8T>G rs2151424618
NM_001166108.2(PALLD):c.2851-10T>C rs1761518453
NM_001166108.2(PALLD):c.2851-6A>G rs1347888847
NM_001166108.2(PALLD):c.2853C>T (p.Val951=)
NM_001166108.2(PALLD):c.2874T>C (p.Asp958=) rs2126494210
NM_001166108.2(PALLD):c.2916T>C (p.Ser972=) rs566543059
NM_001166108.2(PALLD):c.2943C>T (p.Asn981=)
NM_001166108.2(PALLD):c.2949G>A (p.Val983=)
NM_001166108.2(PALLD):c.2988C>A (p.Ala996=)
NM_001166108.2(PALLD):c.3003T>C (p.Cys1001=)
NM_001166108.2(PALLD):c.3016C>A (p.Arg1006=) rs1304987799
NM_001166108.2(PALLD):c.3045G>A (p.Glu1015=)
NM_001166108.2(PALLD):c.3058+15G>A
NM_001166108.2(PALLD):c.3059-13C>T
NM_001166108.2(PALLD):c.3059-20T>C
NM_001166108.2(PALLD):c.3059-6T>C
NM_001166108.2(PALLD):c.3069A>G (p.Ala1023=) rs2126572022
NM_001166108.2(PALLD):c.3150A>G (p.Val1050=) rs781516286
NM_001166108.2(PALLD):c.3186A>G (p.Lys1062=)
NM_001166108.2(PALLD):c.3222G>C (p.Val1074=)
NM_001166108.2(PALLD):c.3224+18G>A
NM_001166108.2(PALLD):c.3225-16_3225-15del
NM_001166108.2(PALLD):c.3225-18C>G
NM_001166108.2(PALLD):c.3261C>T (p.Leu1087=)
NM_001166108.2(PALLD):c.3288T>C (p.Ala1096=) rs2126589237
NM_001166108.2(PALLD):c.3303G>A (p.Val1101=)
NM_001166108.2(PALLD):c.3333C>T (p.Ser1111=)
NM_001166108.2(PALLD):c.3358+17C>T rs1337504036

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