All variants in the ABHD13 gene

Information The variants shown are described using the NM_032859.2 transcript reference sequence.

216 entries on 3 pages. Showing entries 1 - 100.
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AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DB-ID     

dbSNP ID     

gnomAD frequency     

gnomAD homozygote count     
c.-20-31A>G r.(=) p.(=) g.108881516A>G - - 1/166662 0/83330
c.-20-29_-20-28insTATTGATA r.(=) p.(=) g.108881518_108881519insTATTGATA - rs778049901 2/166802 0/83399
c.-20-20T>C r.(=) p.(=) g.108881527T>C - rs772538544 4/167376 0/83684
c.-20-7T>C r.(=) p.(=) g.108881540T>C - - 1/168638 0/84318
c.-20-6C>T r.(=) p.(=) g.108881541C>T - rs753263043 1/171424 0/85711
c.-20-4C>T r.(=) p.(=) g.108881543C>T - rs199612764 4/171904 0/85948
c.-20-1G>A r.(=) p.(=) g.108881546G>A - rs778397270 1/172346 0/86172
c.-17A>G r.(=) p.(=) g.108881550A>G - rs567266304 1/173122 0/86560
c.-15T>G r.(=) p.(=) g.108881552T>G - - 1/174064 0/87031
c.-13dupA r.(=) p.(=) g.108881553_108881554insA - rs779448604 1/174024 0/87011
c.-12C>A r.(=) p.(=) g.108881555C>A - - 1/174112 0/87055
c.-8G>A r.(=) p.(=) g.108881559G>A - rs371891144 1/176228 0/88113
c.-3A>G r.(=) p.(=) g.108881564A>G - - 1/177816 0/88907
c.6A>G r.(?) p.(Glu2=) g.108881572A>G - rs758068537 1/180014 0/90006
c.10T>C r.(?) p.(Ser4Pro) g.108881576T>C - rs779802711 3/186802 0/93398
c.13T>C r.(?) p.(Trp5Arg) g.108881579T>C - rs537159280 1/189012 0/94505
c.30T>C r.(?) p.(Phe10=) g.108881596T>C - - 1/200742 0/100370
c.31G>A r.(?) p.(Val11Ile) g.108881597G>A - - 1/201980 0/100989
c.45A>G r.(?) p.(Leu15=) g.108881611A>G - - 1/216056 0/108027
c.46A>G r.(?) p.(Ile16Val) g.108881612A>G - rs142756657 18/216420 0/108192
c.50C>T r.(?) p.(Ala17Val) g.108881616C>T - rs768560840 1/222934 0/111466
c.65C>G r.(?) p.(Ser22Cys) g.108881631C>G - - 1/237830 0/118914
c.73C>A r.(?) p.(Leu25Ile) g.108881639C>A - rs147102037 15/240708 0/120339
c.91T>C r.(?) p.(Leu31=) g.108881657T>C - - 1/243702 0/121850
c.94C>T r.(?) p.(Pro32Ser) g.108881660C>T - - 1/244524 0/122261
c.111T>C r.(?) p.(Phe37=) g.108881677T>C - - 1/245140 0/122569
c.115C>G r.(?) p.(Leu39Val) g.108881681C>G - - 1/245174 0/122585
c.115C>T r.(?) p.(Leu39=) g.108881681C>T - - 1/245174 0/122585
c.118T>C r.(?) p.(Tyr40His) g.108881684T>C - rs763178879 1/245330 0/122664
c.120T>C r.(?) p.(Tyr40=) g.108881686T>C - rs140080485 1/245310 0/122654
c.128T>A r.(?) p.(Ile43Asn) g.108881694T>A - rs774701319 1/245172 0/122585
c.130A>G r.(?) p.(Ile44Val) g.108881696A>G - - 1/245190 0/122594
c.140T>C r.(?) p.(Leu47Ser) g.108881706T>C - rs759808525 1/244884 0/122441
c.141G>A r.(?) p.(Leu47=) g.108881707G>A - rs374362664 1/244942 0/122470
c.146T>C r.(?) p.(Ile49Thr) g.108881712T>C - rs200506444 31/244922 0/122430
c.151A>G r.(?) p.(Ile51Val) g.108881717A>G - rs756642554 3/244946 0/122470
c.161C>G r.(?) p.(Ala54Gly) g.108881727C>G - rs764678118 1/244772 0/122385
c.163G>A r.(?) p.(Gly55Ser) g.108881729G>A - - 1/244832 0/122415
c.179T>G r.(?) p.(Phe60Cys) g.108881745T>G - rs749911923 1/244702 0/122350
c.180C>T r.(?) p.(Phe60=) g.108881746C>T - rs757961945 2/244538 0/122267
c.183G>A r.(?) p.(Gln61=) g.108881749G>A - rs779563914 1/244500 0/122249
c.187G>A r.(?) p.(Val63Ile) g.108881753G>A - rs191694117 2/244432 0/122214
c.189A>T r.(?) p.(Val63=) g.108881755A>T - rs138545969 19/244436 0/122198
c.189A>G r.(?) p.(Val63=) g.108881755A>G - rs138545969 1/244436 0/122198
c.207A>G r.(?) p.(Glu69=) g.108881773A>G - rs781166861 1/244694 0/122346
c.213A>G r.(?) p.(Pro71=) g.108881779A>G - - 1/245104 0/122551
c.215C>G r.(?) p.(Ser72Cys) g.108881781C>G - rs748052769 1/245098 0/122548
c.216C>T r.(?) p.(Ser72=) g.108881782C>T - rs142014790 2/245046 0/122521
c.223C>T r.(?) p.(Arg75Cys) g.108881789C>T - rs777901033 1/245248 0/122623
c.226C>G r.(?) p.(Leu76Val) g.108881792C>G - rs749374616 2/245360 0/122678
c.228T>G r.(?) p.(Leu76=) g.108881794T>G - rs771100634 1/245380 0/122689
c.230A>G r.(?) p.(Tyr77Cys) g.108881796A>G - rs774381481 1/245388 0/122693
c.234T>A r.(?) p.(Val78=) g.108881800T>A - rs759810157 2/245478 0/122737
c.235C>T r.(?) p.(Pro79Ser) g.108881801C>T - rs772283326 2/245492 0/122744
c.237C>T r.(?) p.(Pro79=) g.108881803C>T - - 1/245488 0/122743
c.239T>C r.(?) p.(Met80Thr) g.108881805T>C - - 1/245550 0/122774
c.243C>T r.(?) p.(Pro81=) g.108881809C>T - rs183867291 8/245548 0/122766
c.249C>T r.(?) p.(Gly83=) g.108881815C>T - rs761076620 2/245586 0/122791
c.251T>G r.(?) p.(Ile84Ser) g.108881817T>G - - 2/245618 0/122807
c.257A>G r.(?) p.(His86Arg) g.108881823A>G - - 2/245642 0/122819
c.265A>G r.(?) p.(Ile89Val) g.108881831A>G - rs754404874 2/245666 0/122831
c.266T>C r.(?) p.(Ile89Thr) g.108881832T>C - rs762353459 1/245646 0/122822
c.275G>T r.(?) p.(Arg92Ile) g.108881841G>T - - 1/245678 0/122838
c.284A>G r.(?) p.(Asp95Gly) g.108881850A>G - - 2/245678 0/122837
c.292C>T r.(?) p.(Arg98Cys) g.108881858C>T - rs150882242 52/245656 0/122776
c.293G>A r.(?) p.(Arg98His) g.108881859G>A - rs139350774 129/245638 0/122690
c.304A>G r.(?) p.(Ile102Val) g.108881870A>G - rs781043841 3/245580 0/122787
c.305T>C r.(?) p.(Ile102Thr) g.108881871T>C - rs762302018 6/245562 0/122775
c.310A>G r.(?) p.(Ile104Val) g.108881876A>G - rs756040875 1/245560 0/122779
c.314G>A r.(?) p.(Arg105Gln) g.108881880G>A - rs749263953 2/245478 0/122737
c.318C>T r.(?) p.(Tyr106=) g.108881884C>T - - 1/245452 0/122725
c.320C>T r.(?) p.(Thr107Ile) g.108881886C>T - rs770850657 5/245448 0/122719
c.323G>A r.(?) p.(Gly108Glu) g.108881889G>A - rs367925617 6/245422 0/122705
c.327C>A r.(?) p.(Asp109Glu) g.108881893C>A - rs199630755 3/245380 0/122687
c.334C>T r.(?) p.(Pro112Ser) g.108881900C>T - rs772260350 42/245290 0/122603
c.337T>C r.(?) p.(Tyr113His) g.108881903T>C - rs775729168 0/245288 0/122643
c.337T>G r.(?) p.(Tyr113Asp) g.108881903T>G - rs775729168 1/245288 0/122643
c.338A>G r.(?) p.(Tyr113Cys) g.108881904A>G - rs761019660 2/245266 0/122631
c.342C>A r.(?) p.(Ser114=) g.108881908C>A - rs769063127 1/245202 0/122600
c.346A>G r.(?) p.(Thr116Ala) g.108881912A>G - rs777062104 3/245204 0/122599
c.349A>G r.(?) p.(Ile117Val) g.108881915A>G - rs762383065 2/245168 0/122582
c.363T>C r.(?) p.(His121=) g.108881929T>C - rs145406609 6/245050 0/122519
c.379A>G r.(?) p.(Ile127Val) g.108881945A>G - rs751061168 1/245024 0/122511
c.388A>C r.(?) p.(Arg130=) g.108881954A>C - rs757083564 2/244914 0/122455
c.394C>T r.(?) p.(Pro132Ser) g.108881960C>T - rs767278268 2/244860 0/122428
c.399T>C r.(?) p.(Asn133=) g.108881965T>C - - 1/244894 0/122446
c.405A>G r.(?) p.(Leu135=) g.108881971A>G - rs752456357 5/244872 0/122431
c.410T>C r.(?) p.(Met137Thr) g.108881976T>C - rs536138947 2/244818 0/122407
c.411G>A r.(?) p.(Met137Ile) g.108881977G>A - - 2/244782 0/122389
c.416T>C r.(?) p.(Val139Ala) g.108881982T>C - rs777717122 1/244794 0/122396
c.420_432del r.(?) p.(Leu141PhefsTer23) g.108881986_108881998del - rs745987804 1/244782 0/122390
c.421C>G r.(?) p.(Leu141Val) g.108881987C>G - - 1/244766 0/122381
c.429T>C r.(?) p.(Val143=) g.108881995T>C - - 1/244840 0/122418
c.432C>T r.(?) p.(Asn144=) g.108881998C>T - rs367859474 1/244784 0/122389
c.432C>G r.(?) p.(Asn144Lys) g.108881998C>G - rs367859474 1/244784 0/122389
c.444T>G r.(?) p.(Val148=) g.108882010T>G - rs200303841 5/244864 0/122427
c.458A>T r.(?) p.(Tyr153Phe) g.108882024A>T - rs757239772 1/244900 0/122449
c.459T>C r.(?) p.(Tyr153=) g.108882025T>C - - 1/244856 0/122427
c.465A>C r.(?) p.(Lys155Asn) g.108882031A>C - rs778763781 1/245018 0/122508
c.467G>C r.(?) p.(Ser156Thr) g.108882033G>C - rs745927939 1/244944 0/122471
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