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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 114

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HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.*317A>T	rs542531106	0.23477
NM_001166108.2(PALLD):c.3359-4G>A	rs112116419	0.01852
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.2199+8G>A	rs200060953	0.00070
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.2891A>C (p.Asp964Ala)	rs750112132	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.2867C>T (p.Thr956Ile)	rs371498362	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.3145C>T (p.Arg1049Cys)	rs548068667	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.*333ATA[3]	rs28364802
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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