Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.209618471_209618502delinsCCTGCAACCGGCGGGCACGCGCAATGTCCTGC | CA1148245821 | LAMB3 | c.2859_2890delinsGCAGGACATTGCGCGTGCCCGCCGGTTGCAGG (p.Lys953=) c.66_97delinsGCAGGACATTGCGCGTGCCCGCCGGTTGCAGG (p.Lys22=) c.2667_2698delinsGCAGGACATTGCGCGTGCCCGCCGGTTGCAGG (p.Lys889=) | |
1 | g.209618476_209618502del | CA1375069 | LAMB3 | c.2864_2890del (p.Asp955_Gln963del) c.71_97del (p.Asp24_Gln32del) c.2672_2698del (p.Asp891_Gln899del) | ClinVar dbSNP ExAC gnomAD v2 |
1 | g.209618499_209618500delinsCT | CA2484296275 | LAMB3 | c.2861_2862delinsAG (p.Gln954=) c.68_69delinsAG (p.Gln23=) c.2669_2670delinsAG (p.Gln890=) | |
1 | g.209618500del | CA36750149 | LAMB3 | c.2861del (p.Gln954ArgfsTer?) c.68del (p.Gln23ArgfsTer?) c.2669del (p.Gln890ArgfsTer?) | dbSNP gnomAD v4 |
1 | g.209618500T>A | CA344585043 | LAMB3 | c.2861A>T (p.Gln954Leu) c.68A>T (p.Gln23Leu) c.2669A>T (p.Gln890Leu) | |
1 | g.209618500T>C | CA344585044 | LAMB3 | c.2861A>G (p.Gln954Arg) c.68A>G (p.Gln23Arg) c.2669A>G (p.Gln890Arg) | |
1 | g.209618500T>G | CA344585045 | LAMB3 | c.2861A>C (p.Gln954Pro) c.68A>C (p.Gln23Pro) c.2669A>C (p.Gln890Pro) | |
1 | g.209618501G>A | CA344585046 | LAMB3 | c.2860C>T (p.Gln954Ter) c.67C>T (p.Gln23Ter) c.2668C>T (p.Gln890Ter) | gnomAD v4 |
1 | g.209618501G>C | CA344585047 | LAMB3 | c.2860C>G (p.Gln954Glu) c.67C>G (p.Gln23Glu) c.2668C>G (p.Gln890Glu) | gnomAD v4 |
1 | g.209618501G>T | CA344585048 | LAMB3 | c.2860C>A (p.Gln954Lys) c.67C>A (p.Gln23Lys) c.2668C>A (p.Gln890Lys) | |
1 | g.209618502C>A | CA344585049 | LAMB3 | c.2859G>T (p.Lys953Asn) c.66G>T (p.Lys22Asn) c.2667G>T (p.Lys889Asn) | |
1 | g.209618502C>G | CA344585050 | LAMB3 | c.2859G>C (p.Lys953Asn) c.66G>C (p.Lys22Asn) c.2667G>C (p.Lys889Asn) | |
1 | g.209618502C>T | CA423029983 | LAMB3 | c.2859G>A (p.Lys953=) c.66G>A (p.Lys22=) c.2667G>A (p.Lys889=) | |
1 | g.209618503T>A | CA344585051 | LAMB3 | c.2858A>T (p.Lys953Met) c.65A>T (p.Lys22Met) c.2666A>T (p.Lys889Met) | |
1 | g.209618503T>C | CA344585052 | LAMB3 | c.2858A>G (p.Lys953Arg) c.65A>G (p.Lys22Arg) c.2666A>G (p.Lys889Arg) | |
1 | g.209618503T>G | CA344585053 | LAMB3 | c.2858A>C (p.Lys953Thr) c.65A>C (p.Lys22Thr) c.2666A>C (p.Lys889Thr) | |
1 | g.209618504T>A | CA344585054 | LAMB3 | c.2857A>T (p.Lys953Ter) c.64A>T (p.Lys22Ter) c.2665A>T (p.Lys889Ter) | |
1 | g.209618504T>C | CA344585055 | LAMB3 | c.2857A>G (p.Lys953Glu) c.64A>G (p.Lys22Glu) c.2665A>G (p.Lys889Glu) | |
1 | g.209618504T>G | CA344585056 | LAMB3 | c.2857A>C (p.Lys953Gln) c.64A>C (p.Lys22Gln) c.2665A>C (p.Lys889Gln) | |
1 | g.209618505G>A | CA423029987 | LAMB3 | c.2856C>T (p.Thr952=) c.63C>T (p.Thr21=) c.2664C>T (p.Thr888=) | |
1 | g.209618505G>C | CA423029989 | LAMB3 | c.2856C>G (p.Thr952=) c.63C>G (p.Thr21=) c.2664C>G (p.Thr888=) | |
1 | g.209618505G>T | CA423029992 | LAMB3 | c.2856C>A (p.Thr952=) c.63C>A (p.Thr21=) c.2664C>A (p.Thr888=) | gnomAD v4 |
1 | g.209618505_209618506delinsAA | CA645532773 | LAMB3 | c.2855_2856delinsTT (p.Thr952Ile) c.62_63delinsTT (p.Thr21Ile) c.2663_2664delinsTT (p.Thr888Ile) | COSMIC |
1 | g.209618506dup | CA2839808583 | LAMB3 | c.2856dup (p.Lys953GlnfsTer13) c.63dup (p.Lys22GlnfsTer13) c.2664dup (p.Lys889GlnfsTer13) | |
1 | g.209618506G>A | CA344585058 | LAMB3 | c.2855C>T (p.Thr952Ile) c.62C>T (p.Thr21Ile) c.2663C>T (p.Thr888Ile) | |
1 | g.209618506G>C | CA344585057 | LAMB3 | c.2855C>G (p.Thr952Ser) c.62C>G (p.Thr21Ser) c.2663C>G (p.Thr888Ser) | gnomAD v4 |
1 | g.209618506G= | CA2484296276 | LAMB3 | c.2855C= (p.Thr952=) c.62C= (p.Thr21=) c.2663C= (p.Thr888=) | |
1 | g.209618506G>T | CA1375080 | LAMB3 | c.2855C>A (p.Thr952Asn) c.62C>A (p.Thr21Asn) c.2663C>A (p.Thr888Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209618507T>A | CA344585059 | LAMB3 | c.2854A>T (p.Thr952Ser) c.61A>T (p.Thr21Ser) c.2662A>T (p.Thr888Ser) | |
1 | g.209618507T>C | CA344585060 | LAMB3 | c.2854A>G (p.Thr952Ala) c.61A>G (p.Thr21Ala) c.2662A>G (p.Thr888Ala) | dbSNP |
1 | g.209618507T>G | CA344585061 | LAMB3 | c.2854A>C (p.Thr952Pro) c.61A>C (p.Thr21Pro) c.2662A>C (p.Thr888Pro) | dbSNP gnomAD v4 |
1 | g.209618507T= | CA2484296277 | LAMB3 | c.2854A= (p.Thr952=) c.61A= (p.Thr21=) c.2662A= (p.Thr888=) | |
1 | g.209618508C>A | CA344585062 | LAMB3 | c.2853G>T (p.Gln951His) c.60G>T (p.Gln20His) c.2661G>T (p.Gln887His) | |
1 | g.209618508C>G | CA344585063 | LAMB3 | c.2853G>C (p.Gln951His) c.60G>C (p.Gln20His) c.2661G>C (p.Gln887His) | |
1 | g.209618508C>T | CA423029999 | LAMB3 | c.2853G>A (p.Gln951=) c.60G>A (p.Gln20=) c.2661G>A (p.Gln887=) | |
1 | g.209618509T>A | CA344585064 | LAMB3 | c.2852A>T (p.Gln951Leu) c.59A>T (p.Gln20Leu) c.2660A>T (p.Gln887Leu) | dbSNP |
1 | g.209618509T>C | CA344585065 | LAMB3 | c.2852A>G (p.Gln951Arg) c.59A>G (p.Gln20Arg) c.2660A>G (p.Gln887Arg) | |
1 | g.209618509T>G | CA344585066 | LAMB3 | c.2852A>C (p.Gln951Pro) c.59A>C (p.Gln20Pro) c.2660A>C (p.Gln887Pro) | |
1 | g.209618509T= | CA2484296278 | LAMB3 | c.2852A= (p.Gln951=) c.59A= (p.Gln20=) c.2660A= (p.Gln887=) | |
1 | g.209618510G>A | CA344585067 | LAMB3 | c.2851C>T (p.Gln951Ter) c.58C>T (p.Gln20Ter) c.2659C>T (p.Gln887Ter) | |
1 | g.209618510G>C | CA344585068 | LAMB3 | c.2851C>G (p.Gln951Glu) c.58C>G (p.Gln20Glu) c.2659C>G (p.Gln887Glu) | |
1 | g.209618510G>T | CA344585069 | LAMB3 | c.2851C>A (p.Gln951Lys) c.58C>A (p.Gln20Lys) c.2659C>A (p.Gln887Lys) | |
1 | g.209618511G>A | CA423030005 | LAMB3 | c.2850C>T (p.Ser950=) c.57C>T (p.Ser19=) c.2658C>T (p.Ser886=) | |
1 | g.209618511G>C | CA423030006 | LAMB3 | c.2850C>G (p.Ser950=) c.57C>G (p.Ser19=) c.2658C>G (p.Ser886=) | |
1 | g.209618511G>T | CA423030007 | LAMB3 | c.2850C>A (p.Ser950=) c.57C>A (p.Ser19=) c.2658C>A (p.Ser886=) | |
1 | g.209618512G>A | CA344585072 | LAMB3 | c.2849C>T (p.Ser950Phe) c.56C>T (p.Ser19Phe) c.2657C>T (p.Ser886Phe) | |
1 | g.209618512G>C | CA344585071 | LAMB3 | c.2849C>G (p.Ser950Cys) c.56C>G (p.Ser19Cys) c.2657C>G (p.Ser886Cys) | gnomAD v4 |
1 | g.209618512G>T | CA344585070 | LAMB3 | c.2849C>A (p.Ser950Tyr) c.56C>A (p.Ser19Tyr) c.2657C>A (p.Ser886Tyr) | |
1 | g.209618513A>C | CA344585073 | LAMB3 | c.2848T>G (p.Ser950Ala) c.55T>G (p.Ser19Ala) c.2656T>G (p.Ser886Ala) | |
1 | g.209618513A>G | CA344585074 | LAMB3 | c.2848T>C (p.Ser950Pro) c.55T>C (p.Ser19Pro) c.2656T>C (p.Ser886Pro) | |
1 | g.209618513A>T | CA344585075 | LAMB3 | c.2848T>A (p.Ser950Thr) c.55T>A (p.Ser19Thr) c.2656T>A (p.Ser886Thr) | |
1 | g.209618514C>A | CA423030013 | LAMB3 | c.2847G>T (p.Leu949=) c.54G>T (p.Leu18=) c.2655G>T (p.Leu885=) | |
1 | g.209618514C>G | CA423030014 | LAMB3 | c.2847G>C (p.Leu949=) c.54G>C (p.Leu18=) c.2655G>C (p.Leu885=) | |
1 | g.209618514C>T | CA423030015 | LAMB3 | c.2847G>A (p.Leu949=) c.54G>A (p.Leu18=) c.2655G>A (p.Leu885=) | |
1 | g.209618515A>C | CA344585076 | LAMB3 | c.2846T>G (p.Leu949Arg) c.53T>G (p.Leu18Arg) c.2654T>G (p.Leu885Arg) | |
1 | g.209618515A>G | CA344585077 | LAMB3 | c.2846T>C (p.Leu949Pro) c.53T>C (p.Leu18Pro) c.2654T>C (p.Leu885Pro) | gnomAD v4 |
1 | g.209618515A>T | CA344585078 | LAMB3 | c.2846T>A (p.Leu949Gln) c.53T>A (p.Leu18Gln) c.2654T>A (p.Leu885Gln) | |
1 | g.209618516G>A | CA423030018 | LAMB3 | c.2845C>T (p.Leu949=) c.52C>T (p.Leu18=) c.2653C>T (p.Leu885=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209618516G>C | CA344585079 | LAMB3 | c.2845C>G (p.Leu949Val) c.52C>G (p.Leu18Val) c.2653C>G (p.Leu885Val) | |
1 | g.209618516G= | CA2484296279 | LAMB3 | c.2845C= (p.Leu949=) c.52C= (p.Leu18=) c.2653C= (p.Leu885=) | |
1 | g.209618516G>T | CA344585080 | LAMB3 | c.2845C>A (p.Leu949Met) c.52C>A (p.Leu18Met) c.2653C>A (p.Leu885Met) | |
1 | g.209618517C>A | CA423030023 | LAMB3 | c.2844G>T (p.Val948=) c.51G>T (p.Val17=) c.2652G>T (p.Val884=) | |
1 | g.209618517C>G | CA423030021 | LAMB3 | c.2844G>C (p.Val948=) c.51G>C (p.Val17=) c.2652G>C (p.Val884=) | |
1 | g.209618517C>T | CA423030020 | LAMB3 | c.2844G>A (p.Val948=) c.51G>A (p.Val17=) c.2652G>A (p.Val884=) | |
1 | g.209618518A>C | CA344585081 | LAMB3 | c.2843T>G (p.Val948Gly) c.50T>G (p.Val17Gly) c.2651T>G (p.Val884Gly) | |
1 | g.209618518A>G | CA344585082 | LAMB3 | c.2843T>C (p.Val948Ala) c.50T>C (p.Val17Ala) c.2651T>C (p.Val884Ala) | |
1 | g.209618518A>T | CA344585083 | LAMB3 | c.2843T>A (p.Val948Glu) c.50T>A (p.Val17Glu) c.2651T>A (p.Val884Glu) | |
1 | g.209618518_209618519delinsAC | CA2484296280 | LAMB3 | c.2842_2843delinsGT (p.Val948=) c.49_50delinsGT (p.Val17=) c.2650_2651delinsGT (p.Val884=) | |
1 | g.209618519C>A | CA344585085 | LAMB3 | c.2842G>T (p.Val948Leu) c.49G>T (p.Val17Leu) c.2650G>T (p.Val884Leu) | |
1 | g.209618519C= | CA2484296281 | LAMB3 | c.2842G= (p.Val948=) c.49G= (p.Val17=) c.2650G= (p.Val884=) | |
1 | g.209618519C>G | CA344585084 | LAMB3 | c.2842G>C (p.Val948Leu) c.49G>C (p.Val17Leu) c.2650G>C (p.Val884Leu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209618519C>T | CA344585086 | LAMB3 | c.2842G>A (p.Val948Met) c.49G>A (p.Val17Met) c.2650G>A (p.Val884Met) | gnomAD v4 |
1 | g.209618520del | CA1375081 | LAMB3 | c.2842del (p.Val948CysfsTer?) c.49del (p.Val17CysfsTer?) c.2650del (p.Val884CysfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618520C>A | CA344585087 | LAMB3 | c.2841G>T (p.Leu947Phe) c.48G>T (p.Leu16Phe) c.2649G>T (p.Leu883Phe) | |
1 | g.209618520C= | CA1141986146 | LAMB3 | c.2841G= (p.Leu947=) c.48G= (p.Leu16=) c.2649G= (p.Leu883=) | |
1 | g.209618520C>G | CA344585088 | LAMB3 | c.2841G>C (p.Leu947Phe) c.48G>C (p.Leu16Phe) c.2649G>C (p.Leu883Phe) | |
1 | g.209618520C>T | CA1375082 | LAMB3 | c.2841G>A (p.Leu947=) c.48G>A (p.Leu16=) c.2649G>A (p.Leu883=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618521A>C | CA344585091 | LAMB3 | c.2840T>G (p.Leu947Trp) c.47T>G (p.Leu16Trp) c.2648T>G (p.Leu883Trp) | |
1 | g.209618521A>G | CA344585090 | LAMB3 | c.2840T>C (p.Leu947Ser) c.47T>C (p.Leu16Ser) c.2648T>C (p.Leu883Ser) | gnomAD v4 |
1 | g.209618521A>T | CA344585089 | LAMB3 | c.2840T>A (p.Leu947Ter) c.47T>A (p.Leu16Ter) c.2648T>A (p.Leu883Ter) | |
1 | g.209618522A>C | CA344585092 | LAMB3 | c.2839T>G (p.Leu947Val) c.46T>G (p.Leu16Val) c.2647T>G (p.Leu883Val) | |
1 | g.209618522A>G | CA423030030 | LAMB3 | c.2839T>C (p.Leu947=) c.46T>C (p.Leu16=) c.2647T>C (p.Leu883=) | |
1 | g.209618522A>T | CA344585093 | LAMB3 | c.2839T>A (p.Leu947Met) c.46T>A (p.Leu16Met) c.2647T>A (p.Leu883Met) | |
1 | g.209618523G>A | CA423030031 | LAMB3 | c.2838C>T (p.Asp946=) c.45C>T (p.Asp15=) c.2646C>T (p.Asp882=) | |
1 | g.209618523G>C | CA344585094 | LAMB3 | c.2838C>G (p.Asp946Glu) c.45C>G (p.Asp15Glu) c.2646C>G (p.Asp882Glu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209618523G= | CA2484296282 | LAMB3 | c.2838C= (p.Asp946=) c.45C= (p.Asp15=) c.2646C= (p.Asp882=) | |
1 | g.209618523G>T | CA344585095 | LAMB3 | c.2838C>A (p.Asp946Glu) c.45C>A (p.Asp15Glu) c.2646C>A (p.Asp882Glu) | |
1 | g.209618524T>A | CA344585096 | LAMB3 | c.2837A>T (p.Asp946Val) c.44A>T (p.Asp15Val) c.2645A>T (p.Asp882Val) | |
1 | g.209618524T>C | CA344585097 | LAMB3 | c.2837A>G (p.Asp946Gly) c.44A>G (p.Asp15Gly) c.2645A>G (p.Asp882Gly) | |
1 | g.209618524T>G | CA344585098 | LAMB3 | c.2837A>C (p.Asp946Ala) c.44A>C (p.Asp15Ala) c.2645A>C (p.Asp882Ala) | |
1 | g.209618525C>A | CA344585101 | LAMB3 | c.2836G>T (p.Asp946Tyr) c.43G>T (p.Asp15Tyr) c.2644G>T (p.Asp882Tyr) | |
1 | g.209618525C>G | CA344585100 | LAMB3 | c.2836G>C (p.Asp946His) c.43G>C (p.Asp15His) c.2644G>C (p.Asp882His) | |
1 | g.209618525C>T | CA344585099 | LAMB3 | c.2836G>A (p.Asp946Asn) c.43G>A (p.Asp15Asn) c.2644G>A (p.Asp882Asn) | COSMIC |
1 | g.209618526C>A | CA423030037 | LAMB3 | c.2835G>T (p.Val945=) c.42G>T (p.Val14=) c.2643G>T (p.Val881=) | |
1 | g.209618526C>G | CA423030038 | LAMB3 | c.2835G>C (p.Val945=) c.42G>C (p.Val14=) c.2643G>C (p.Val881=) | |
1 | g.209618526C>T | CA423030039 | LAMB3 | c.2835G>A (p.Val945=) c.42G>A (p.Val14=) c.2643G>A (p.Val881=) | |
1 | g.209618527A>C | CA344585103 | LAMB3 | c.2834T>G (p.Val945Gly) c.41T>G (p.Val14Gly) c.2642T>G (p.Val881Gly) | |
1 | g.209618527A>G | CA344585102 | LAMB3 | c.2834T>C (p.Val945Ala) c.41T>C (p.Val14Ala) c.2642T>C (p.Val881Ala) | |
1 | g.209618527A>T | CA344585104 | LAMB3 | c.2834T>A (p.Val945Glu) c.41T>A (p.Val14Glu) c.2642T>A (p.Val881Glu) | |
1 | g.209618528C>A | CA1375084 | LAMB3 | c.2833G>T (p.Val945Leu) c.40G>T (p.Val14Leu) c.2641G>T (p.Val881Leu) | dbSNP ExAC gnomAD v2 |
1 | g.209618528C= | CA2484296283 | LAMB3 | c.2833G= (p.Val945=) c.40G= (p.Val14=) c.2641G= (p.Val881=) | |
1 | g.209618528C>G | CA344585105 | LAMB3 | c.2833G>C (p.Val945Leu) c.40G>C (p.Val14Leu) c.2641G>C (p.Val881Leu) | gnomAD v4 |
1 | g.209618528C>T | CA1375083 | LAMB3 | c.2833G>A (p.Val945Met) c.40G>A (p.Val14Met) c.2641G>A (p.Val881Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618529G>A | CA1375085 | LAMB3 | c.2832C>T (p.Asn944=) c.39C>T (p.Asn13=) c.2640C>T (p.Asn880=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618529G>C | CA344585106 | LAMB3 | c.2832C>G (p.Asn944Lys) c.39C>G (p.Asn13Lys) c.2640C>G (p.Asn880Lys) | |
1 | g.209618529G= | CA1141248731 | LAMB3 | c.2832C= (p.Asn944=) c.39C= (p.Asn13=) c.2640C= (p.Asn880=) | |
1 | g.209618529G>T | CA344585107 | LAMB3 | c.2832C>A (p.Asn944Lys) c.39C>A (p.Asn13Lys) c.2640C>A (p.Asn880Lys) | |
1 | g.209618530T>A | CA344585109 | LAMB3 | c.2831A>T (p.Asn944Ile) c.38A>T (p.Asn13Ile) c.2639A>T (p.Asn880Ile) | |
1 | g.209618530T>C | CA1375086 | LAMB3 | c.2831A>G (p.Asn944Ser) c.38A>G (p.Asn13Ser) c.2639A>G (p.Asn880Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618530T>G | CA344585108 | LAMB3 | c.2831A>C (p.Asn944Thr) c.38A>C (p.Asn13Thr) c.2639A>C (p.Asn880Thr) | dbSNP gnomAD v4 |
1 | g.209618530T= | CA1147322938 | LAMB3 | c.2831A= (p.Asn944=) c.38A= (p.Asn13=) c.2639A= (p.Asn880=) | |
1 | g.209618531dup | CA2839276473 | LAMB3 | c.2831dup (p.Asn944LysfsTer22) c.38dup (p.Asn13LysfsTer22) c.2639dup (p.Asn880LysfsTer22) | |
1 | g.209618531T>A | CA344585110 | LAMB3 | c.2830A>T (p.Asn944Tyr) c.37A>T (p.Asn13Tyr) c.2638A>T (p.Asn880Tyr) | |
1 | g.209618531T>C | CA344585111 | LAMB3 | c.2830A>G (p.Asn944Asp) c.37A>G (p.Asn13Asp) c.2638A>G (p.Asn880Asp) | |
1 | g.209618531T>G | CA344585112 | LAMB3 | c.2830A>C (p.Asn944His) c.37A>C (p.Asn13His) c.2638A>C (p.Asn880His) | |
1 | g.209618532G>A | CA423030046 | LAMB3 | c.2829C>T (p.Pro943=) c.36C>T (p.Pro12=) c.2637C>T (p.Pro879=) | |
1 | g.209618532G>C | CA423030047 | LAMB3 | c.2829C>G (p.Pro943=) c.36C>G (p.Pro12=) c.2637C>G (p.Pro879=) | |
1 | g.209618532G>T | CA423030048 | LAMB3 | c.2829C>A (p.Pro943=) c.36C>A (p.Pro12=) c.2637C>A (p.Pro879=) | |
1 | g.209618533G>A | CA344585113 | LAMB3 | c.2828C>T (p.Pro943Leu) c.35C>T (p.Pro12Leu) c.2636C>T (p.Pro879Leu) | |
1 | g.209618533G>C | CA1375087 | LAMB3 | c.2828C>G (p.Pro943Arg) c.35C>G (p.Pro12Arg) c.2636C>G (p.Pro879Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209618533G= | CA1149114322 | LAMB3 | c.2828C= (p.Pro943=) c.35C= (p.Pro12=) c.2636C= (p.Pro879=) | |
1 | g.209618533G>T | CA344585114 | LAMB3 | c.2828C>A (p.Pro943His) c.35C>A (p.Pro12His) c.2636C>A (p.Pro879His) | |
1 | g.209618534G>A | CA344585116 | LAMB3 | c.2827C>T (p.Pro943Ser) c.34C>T (p.Pro12Ser) c.2635C>T (p.Pro879Ser) | |
1 | g.209618534G>C | CA1375088 | LAMB3 | c.2827C>G (p.Pro943Ala) c.34C>G (p.Pro12Ala) c.2635C>G (p.Pro879Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618534G= | CA1142116265 | LAMB3 | c.2827C= (p.Pro943=) c.34C= (p.Pro12=) c.2635C= (p.Pro879=) | |
1 | g.209618534G>T | CA344585115 | LAMB3 | c.2827C>A (p.Pro943Thr) c.34C>A (p.Pro12Thr) c.2635C>A (p.Pro879Thr) | |
1 | g.209618535G>A | CA423030049 | LAMB3 | c.2826C>T (p.Leu942=) c.33C>T (p.Leu11=) c.2634C>T (p.Leu878=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
1 | g.209618535G>C | CA423030050 | LAMB3 | c.2826C>G (p.Leu942=) c.33C>G (p.Leu11=) c.2634C>G (p.Leu878=) | |
1 | g.209618535G= | CA2484296284 | LAMB3 | c.2826C= (p.Leu942=) c.33C= (p.Leu11=) c.2634C= (p.Leu878=) | |
1 | g.209618535G>T | CA423030051 | LAMB3 | c.2826C>A (p.Leu942=) c.33C>A (p.Leu11=) c.2634C>A (p.Leu878=) | |
1 | g.209618536A>C | CA344585117 | LAMB3 | c.2825T>G (p.Leu942Arg) c.32T>G (p.Leu11Arg) c.2633T>G (p.Leu878Arg) | |
1 | g.209618536A>G | CA344585118 | LAMB3 | c.2825T>C (p.Leu942Pro) c.32T>C (p.Leu11Pro) c.2633T>C (p.Leu878Pro) | gnomAD v4 |
1 | g.209618536A>T | CA344585119 | LAMB3 | c.2825T>A (p.Leu942His) c.32T>A (p.Leu11His) c.2633T>A (p.Leu878His) | |
1 | g.209618537G>A | CA344585120 | LAMB3 | c.2824C>T (p.Leu942Phe) c.31C>T (p.Leu11Phe) c.2632C>T (p.Leu878Phe) | |
1 | g.209618537G>C | CA344585121 | LAMB3 | c.2824C>G (p.Leu942Val) c.31C>G (p.Leu11Val) c.2632C>G (p.Leu878Val) | |
1 | g.209618537G= | CA2484296285 | LAMB3 | c.2824C= (p.Leu942=) c.31C= (p.Leu11=) c.2632C= (p.Leu878=) | |
1 | g.209618537G>T | CA36750206 | LAMB3 | c.2824C>A (p.Leu942Ile) c.31C>A (p.Leu11Ile) c.2632C>A (p.Leu878Ile) | dbSNP |
1 | g.209618538C>A | CA344585122 | LAMB3 | c.2823G>T (p.Arg941Ser) c.30G>T (p.Arg10Ser) c.2631G>T (p.Arg877Ser) | |
1 | g.209618538C= | CA1144199222 | LAMB3 | c.2823G= (p.Arg941=) c.30G= (p.Arg10=) c.2631G= (p.Arg877=) | |
1 | g.209618538C>G | CA36750213 | LAMB3 | c.2823G>C (p.Arg941Ser) c.30G>C (p.Arg10Ser) c.2631G>C (p.Arg877Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618538C>T | CA423030052 | LAMB3 | c.2823G>A (p.Arg941=) c.30G>A (p.Arg10=) c.2631G>A (p.Arg877=) | dbSNP gnomAD v4 |
1 | g.209618539del | CA2697554864 | LAMB3 | c.2823del (p.Arg941SerfsTer?) c.30del (p.Arg10SerfsTer?) c.2631del (p.Arg877SerfsTer?) | ClinVar |
1 | g.209618539C>A | CA344585123 | LAMB3 | c.2822G>T (p.Arg941Met) c.29G>T (p.Arg10Met) c.2630G>T (p.Arg877Met) | |
1 | g.209618539C>G | CA344585124 | LAMB3 | c.2822G>C (p.Arg941Thr) c.29G>C (p.Arg10Thr) c.2630G>C (p.Arg877Thr) | |
1 | g.209618539C>T | CA344585125 | LAMB3 | c.2822G>A (p.Arg941Lys) c.29G>A (p.Arg10Lys) c.2630G>A (p.Arg877Lys) | |
1 | g.209618540T>A | CA344585126 | LAMB3 | c.2821A>T (p.Arg941Trp) c.28A>T (p.Arg10Trp) c.2629A>T (p.Arg877Trp) | |
1 | g.209618540T>C | CA344585127 | LAMB3 | c.2821A>G (p.Arg941Gly) c.28A>G (p.Arg10Gly) c.2629A>G (p.Arg877Gly) | |
1 | g.209618540T>G | CA423030055 | LAMB3 | c.2821A>C (p.Arg941=) c.28A>C (p.Arg10=) c.2629A>C (p.Arg877=) | |
1 | g.209618541G>A | CA423030061 | LAMB3 | c.2820C>T (p.Ala940=) c.27C>T (p.Ala9=) c.2628C>T (p.Ala876=) | |
1 | g.209618541G>C | CA423030060 | LAMB3 | c.2820C>G (p.Ala940=) c.27C>G (p.Ala9=) c.2628C>G (p.Ala876=) | |
1 | g.209618541G>T | CA423030057 | LAMB3 | c.2820C>A (p.Ala940=) c.27C>A (p.Ala9=) c.2628C>A (p.Ala876=) | |
1 | g.209618542G>A | CA344585128 | LAMB3 | c.2819C>T (p.Ala940Val) c.26C>T (p.Ala9Val) c.2627C>T (p.Ala876Val) | gnomAD v4 |
1 | g.209618542G>C | CA344585130 | LAMB3 | c.2819C>G (p.Ala940Gly) c.26C>G (p.Ala9Gly) c.2627C>G (p.Ala876Gly) | |
1 | g.209618542G>T | CA344585129 | LAMB3 | c.2819C>A (p.Ala940Asp) c.26C>A (p.Ala9Asp) c.2627C>A (p.Ala876Asp) | |
1 | g.209618543C>A | CA344585131 | LAMB3 | c.2818G>T (p.Ala940Ser) c.25G>T (p.Ala9Ser) c.2626G>T (p.Ala876Ser) | |
1 | g.209618543C= | CA2484296286 | LAMB3 | c.2818G= (p.Ala940=) c.25G= (p.Ala9=) c.2626G= (p.Ala876=) | |
1 | g.209618543C>G | CA344585132 | LAMB3 | c.2818G>C (p.Ala940Pro) c.25G>C (p.Ala9Pro) c.2626G>C (p.Ala876Pro) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209618543C>T | CA344585133 | LAMB3 | c.2818G>A (p.Ala940Thr) c.25G>A (p.Ala9Thr) c.2626G>A (p.Ala876Thr) | gnomAD v4 |
1 | g.209618544T>A | CA423030064 | LAMB3 | c.2817A>T (p.Ala939=) c.24A>T (p.Ala8=) c.2625A>T (p.Ala875=) | |
1 | g.209618544T>C | CA423030066 | LAMB3 | c.2817A>G (p.Ala939=) c.24A>G (p.Ala8=) c.2625A>G (p.Ala875=) | |
1 | g.209618544T>G | CA423030065 | LAMB3 | c.2817A>C (p.Ala939=) c.24A>C (p.Ala8=) c.2625A>C (p.Ala875=) | |
1 | g.209618545G>A | CA344585134 | LAMB3 | c.2816C>T (p.Ala939Val) c.23C>T (p.Ala8Val) c.2624C>T (p.Ala875Val) | gnomAD v4 |
1 | g.209618545G>C | CA344585135 | LAMB3 | c.2816C>G (p.Ala939Gly) c.23C>G (p.Ala8Gly) c.2624C>G (p.Ala875Gly) | |
1 | g.209618545G>T | CA344585136 | LAMB3 | c.2816C>A (p.Ala939Glu) c.23C>A (p.Ala8Glu) c.2624C>A (p.Ala875Glu) | |
1 | g.209618546C>A | CA344585137 | LAMB3 | c.2815G>T (p.Ala939Ser) c.22G>T (p.Ala8Ser) c.2623G>T (p.Ala875Ser) | |
1 | g.209618546C= | CA2484296287 | LAMB3 | c.2815G= (p.Ala939=) c.22G= (p.Ala8=) c.2623G= (p.Ala875=) | |
1 | g.209618546C>G | CA344585138 | LAMB3 | c.2815G>C (p.Ala939Pro) c.22G>C (p.Ala8Pro) c.2623G>C (p.Ala875Pro) | |
1 | g.209618546C>T | CA344585139 | LAMB3 | c.2815G>A (p.Ala939Thr) c.22G>A (p.Ala8Thr) c.2623G>A (p.Ala875Thr) | dbSNP gnomAD v4 |
1 | g.209618547A>C | CA344585140 | LAMB3 | c.2814T>G (p.Ile938Met) c.21T>G (p.Ile7Met) c.2622T>G (p.Ile874Met) | |
1 | g.209618547A>G | CA423030070 | LAMB3 | c.2814T>C (p.Ile938=) c.21T>C (p.Ile7=) c.2622T>C (p.Ile874=) | |
1 | g.209618547A>T | CA423030071 | LAMB3 | c.2814T>A (p.Ile938=) c.21T>A (p.Ile7=) c.2622T>A (p.Ile874=) | |
1 | g.209618548A= | CA2484296288 | LAMB3 | c.2813T= (p.Ile938=) c.20T= (p.Ile7=) c.2621T= (p.Ile874=) | |
1 | g.209618548A>C | CA344585141 | LAMB3 | c.2813T>G (p.Ile938Ser) c.20T>G (p.Ile7Ser) c.2621T>G (p.Ile874Ser) | |
1 | g.209618548A>G | CA1375089 | LAMB3 | c.2813T>C (p.Ile938Thr) c.20T>C (p.Ile7Thr) c.2621T>C (p.Ile874Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618548A>T | CA344585142 | LAMB3 | c.2813T>A (p.Ile938Asn) c.20T>A (p.Ile7Asn) c.2621T>A (p.Ile874Asn) | |
1 | g.209618549T>A | CA344585144 | LAMB3 | c.2812A>T (p.Ile938Phe) c.19A>T (p.Ile7Phe) c.2620A>T (p.Ile874Phe) | |
1 | g.209618549T>C | CA1375090 | LAMB3 | c.2812A>G (p.Ile938Val) c.19A>G (p.Ile7Val) c.2620A>G (p.Ile874Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209618549T>G | CA344585143 | LAMB3 | c.2812A>C (p.Ile938Leu) c.19A>C (p.Ile7Leu) c.2620A>C (p.Ile874Leu) | |
1 | g.209618549T= | CA1148897863 | LAMB3 | c.2812A= (p.Ile938=) c.19A= (p.Ile7=) c.2620A= (p.Ile874=) | |
1 | g.209618550G>A | CA423030076 | LAMB3 | c.2811C>T (p.Ala937=) c.18C>T (p.Ala6=) c.2619C>T (p.Ala873=) | |
1 | g.209618550G>C | CA423030077 | LAMB3 | c.2811C>G (p.Ala937=) c.18C>G (p.Ala6=) c.2619C>G (p.Ala873=) | |
1 | g.209618550G>T | CA423030078 | LAMB3 | c.2811C>A (p.Ala937=) c.18C>A (p.Ala6=) c.2619C>A (p.Ala873=) | |
1 | g.209618551G>A | CA344585145 | LAMB3 | c.2810C>T (p.Ala937Val) c.17C>T (p.Ala6Val) c.2618C>T (p.Ala873Val) | gnomAD v4 |
1 | g.209618551G>C | CA344585146 | LAMB3 | c.2810C>G (p.Ala937Gly) c.17C>G (p.Ala6Gly) c.2618C>G (p.Ala873Gly) | |
1 | g.209618551G>T | CA344585147 | LAMB3 | c.2810C>A (p.Ala937Asp) c.17C>A (p.Ala6Asp) c.2618C>A (p.Ala873Asp) | |
1 | g.209618552C>A | CA344585148 | LAMB3 | c.2809G>T (p.Ala937Ser) c.16G>T (p.Ala6Ser) c.2617G>T (p.Ala873Ser) | |
1 | g.209618552C= | CA2484296289 | LAMB3 | c.2809G= (p.Ala937=) c.16G= (p.Ala6=) c.2617G= (p.Ala873=) | |
1 | g.209618552C>G | CA344585149 | LAMB3 | c.2809G>C (p.Ala937Pro) c.16G>C (p.Ala6Pro) c.2617G>C (p.Ala873Pro) | |
1 | g.209618552C>T | CA36750221 | LAMB3 | c.2809G>A (p.Ala937Thr) c.16G>A (p.Ala6Thr) c.2617G>A (p.Ala873Thr) | dbSNP |
1 | g.209618553C>A | CA344585150 | LAMB3 | c.2808G>T (p.Gln936His) c.15G>T (p.Gln5His) c.2616G>T (p.Gln872His) | |
1 | g.209618553C>G | CA344585151 | LAMB3 | c.2808G>C (p.Gln936His) c.15G>C (p.Gln5His) c.2616G>C (p.Gln872His) | |
1 | g.209618553C>T | CA423030083 | LAMB3 | c.2808G>A (p.Gln936=) c.15G>A (p.Gln5=) c.2616G>A (p.Gln872=) | |
1 | g.209618554T>A | CA344585152 | LAMB3 | c.2807A>T (p.Gln936Leu) c.14A>T (p.Gln5Leu) c.2615A>T (p.Gln872Leu) | |
1 | g.209618554T>C | CA344585153 | LAMB3 | c.2807A>G (p.Gln936Arg) c.14A>G (p.Gln5Arg) c.2615A>G (p.Gln872Arg) | |
1 | g.209618554T>G | CA344585154 | LAMB3 | c.2807A>C (p.Gln936Pro) c.14A>C (p.Gln5Pro) c.2615A>C (p.Gln872Pro) | |
1 | g.209618555G>A | CA257280 | LAMB3 | c.2806C>T (p.Gln936Ter) c.13C>T (p.Gln5Ter) c.2614C>T (p.Gln872Ter) | ClinVar dbSNP |
1 | g.209618555G>C | CA344585156 | LAMB3 | c.2806C>G (p.Gln936Glu) c.13C>G (p.Gln5Glu) c.2614C>G (p.Gln872Glu) | |
1 | g.209618555G= | CA1141581351 | LAMB3 | c.2806C= (p.Gln936=) c.13C= (p.Gln5=) c.2614C= (p.Gln872=) | |
1 | g.209618555G>T | CA344585155 | LAMB3 | c.2806C>A (p.Gln936Lys) c.13C>A (p.Gln5Lys) c.2614C>A (p.Gln872Lys) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209618556G>A | CA423030085 | LAMB3 | c.2805C>T (p.Ile935=) c.12C>T (p.Ile4=) c.2613C>T (p.Ile871=) | gnomAD v4 |
1 | g.209618556G>C | CA344585157 | LAMB3 | c.2805C>G (p.Ile935Met) c.12C>G (p.Ile4Met) c.2613C>G (p.Ile871Met) | |
1 | g.209618556G>T | CA423030087 | LAMB3 | c.2805C>A (p.Ile935=) c.12C>A (p.Ile4=) c.2613C>A (p.Ile871=) | |
1 | g.209618557A>C | CA344585160 | LAMB3 | c.2804T>G (p.Ile935Ser) c.11T>G (p.Ile4Ser) c.2612T>G (p.Ile871Ser) | gnomAD v4 |
1 | g.209618557A>G | CA344585158 | LAMB3 | c.2804T>C (p.Ile935Thr) c.11T>C (p.Ile4Thr) c.2612T>C (p.Ile871Thr) | |
1 | g.209618557A>T | CA344585159 | LAMB3 | c.2804T>A (p.Ile935Asn) c.11T>A (p.Ile4Asn) c.2612T>A (p.Ile871Asn) | |
1 | g.209618558T>A | CA36750224 | LAMB3 | c.2803A>T (p.Ile935Phe) c.10A>T (p.Ile4Phe) c.2611A>T (p.Ile871Phe) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209618558T>C | CA344585161 | LAMB3 | c.2803A>G (p.Ile935Val) c.10A>G (p.Ile4Val) c.2611A>G (p.Ile871Val) | |
1 | g.209618558T>G | CA344585162 | LAMB3 | c.2803A>C (p.Ile935Leu) c.10A>C (p.Ile4Leu) c.2611A>C (p.Ile871Leu) | |
1 | g.209618558T= | CA2484296290 | LAMB3 | c.2803A= (p.Ile935=) c.10A= (p.Ile4=) c.2611A= (p.Ile871=) | |
1 | g.209618558dup | CA2840705964 | LAMB3 | c.2803dup (p.Ile935AsnfsTer?) c.10dup (p.Ile4AsnfsTer?) c.2611dup (p.Ile871AsnfsTer?) | |
1 | g.209618559C>A | CA1375091 | LAMB3 | c.2802G>T (p.Glu934Asp) c.9G>T (p.Glu3Asp) c.2610G>T (p.Glu870Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618559C= | CA2484296291 | LAMB3 | c.2802G= (p.Glu934=) c.9G= (p.Glu3=) c.2610G= (p.Glu870=) | |
1 | g.209618559C>G | CA344585163 | LAMB3 | c.2802G>C (p.Glu934Asp) c.9G>C (p.Glu3Asp) c.2610G>C (p.Glu870Asp) | |
1 | g.209618559C>T | CA1375092 | LAMB3 | c.2802G>A (p.Glu934=) c.9G>A (p.Glu3=) c.2610G>A (p.Glu870=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
1 | g.209618560T>A | CA344585164 | LAMB3 | c.2801A>T (p.Glu934Val) c.8A>T (p.Glu3Val) c.2609A>T (p.Glu870Val) | dbSNP |
1 | g.209618560T>C | CA344585165 | LAMB3 | c.2801A>G (p.Glu934Gly) c.8A>G (p.Glu3Gly) c.2609A>G (p.Glu870Gly) | |
1 | g.209618560T>G | CA1375093 | LAMB3 | c.2801A>C (p.Glu934Ala) c.8A>C (p.Glu3Ala) c.2609A>C (p.Glu870Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209618560T= | CA2484296292 | LAMB3 | c.2801A= (p.Glu934=) c.8A= (p.Glu3=) c.2609A= (p.Glu870=) | |
1 | g.209618561del | CA2580061993 | LAMB3 | c.2800del (p.Glu934ArgfsTer?) c.7del (p.Glu3ArgfsTer?) c.2608del (p.Glu870ArgfsTer?) | ClinVar |
1 | g.209618561C>A | CA344585168 | LAMB3 | c.2800G>T (p.Glu934Ter) c.7G>T (p.Glu3Ter) c.2608G>T (p.Glu870Ter) | |
1 | g.209618561C>G | CA344585166 | LAMB3 | c.2800G>C (p.Glu934Gln) c.7G>C (p.Glu3Gln) c.2608G>C (p.Glu870Gln) | |
1 | g.209618561C>T | CA344585167 | LAMB3 | c.2800G>A (p.Glu934Lys) c.7G>A (p.Glu3Lys) c.2608G>A (p.Glu870Lys) | gnomAD v4 |
1 | g.209618562A= | CA2484296293 | LAMB3 | c.2799T= (p.Asn933=) c.6T= (p.Asn2=) c.2607T= (p.Asn869=) | |
1 | g.209618562A>C | CA344585169 | LAMB3 | c.2799T>G (p.Asn933Lys) c.6T>G (p.Asn2Lys) c.2607T>G (p.Asn869Lys) | gnomAD v4 |
1 | g.209618562A>G | CA423030094 | LAMB3 | c.2799T>C (p.Asn933=) c.6T>C (p.Asn2=) c.2607T>C (p.Asn869=) | ClinVar dbSNP |
1 | g.209618562A>T | CA344585170 | LAMB3 | c.2799T>A (p.Asn933Lys) c.6T>A (p.Asn2Lys) c.2607T>A (p.Asn869Lys) | |
1 | g.209618563T>A | CA344585171 | LAMB3 | c.2798A>T (p.Asn933Ile) c.5A>T (p.Asn2Ile) c.2606A>T (p.Asn869Ile) | gnomAD v4 |
1 | g.209618563T>C | CA344585172 | LAMB3 | c.2798A>G (p.Asn933Ser) c.5A>G (p.Asn2Ser) c.2606A>G (p.Asn869Ser) | dbSNP gnomAD v4 |
1 | g.209618563T>G | CA344585173 | LAMB3 | c.2798A>C (p.Asn933Thr) c.5A>C (p.Asn2Thr) c.2606A>C (p.Asn869Thr) | |
1 | g.209618563T= | CA2484296294 | LAMB3 | c.2798A= (p.Asn933=) c.5A= (p.Asn2=) c.2606A= (p.Asn869=) | |
1 | g.209618564T>A | CA344585174 | LAMB3 | c.2797A>T (p.Asn933Tyr) c.4A>T (p.Asn2Tyr) c.2605A>T (p.Asn869Tyr) | |
1 | g.209618564T>C | CA344585175 | LAMB3 | c.2797A>G (p.Asn933Asp) c.4A>G (p.Asn2Asp) c.2605A>G (p.Asn869Asp) | |
1 | g.209618564T>G | CA344585176 | LAMB3 | c.2797A>C (p.Asn933His) c.4A>C (p.Asn2His) c.2605A>C (p.Asn869His) | |
1 | g.209618565C>A | CA344585177 | LAMB3 | c.2796G>T (p.Met932Ile) c.3G>T (p.Met1Ile) c.2604G>T (p.Met868Ile) | |
1 | g.209618565C>G | CA344585178 | LAMB3 | c.2796G>C (p.Met932Ile) c.3G>C (p.Met1Ile) c.2604G>C (p.Met868Ile) | |
1 | g.209618565C>T | CA344585179 | LAMB3 | c.2796G>A (p.Met932Ile) c.3G>A (p.Met1Ile) c.2604G>A (p.Met868Ile) | gnomAD v4 |
1 | g.209618566A= | CA1141705368 | LAMB3 | c.2795T= (p.Met932=) c.2T= (p.Met1=) c.2603T= (p.Met868=) | |
1 | g.209618566A>C | CA344585181 | LAMB3 | c.2795T>G (p.Met932Arg) c.2T>G (p.Met1Arg) c.2603T>G (p.Met868Arg) | |
1 | g.209618566A>G | CA1375094 | LAMB3 | c.2795T>C (p.Met932Thr) c.2T>C (p.Met1Thr) c.2603T>C (p.Met868Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618566A>T | CA344585180 | LAMB3 | c.2795T>A (p.Met932Lys) c.2T>A (p.Met1Lys) c.2603T>A (p.Met868Lys) | |
1 | g.209618567T>A | CA344585182 | LAMB3 | c.2794A>T (p.Met932Leu) c.1A>T (p.Met1Leu) c.2602A>T (p.Met868Leu) | |
1 | g.209618567T>C | CA344585183 | LAMB3 | c.2794A>G (p.Met932Val) c.1A>G (p.Met1Val) c.2602A>G (p.Met868Val) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209618567T>G | CA344585184 | LAMB3 | c.2794A>C (p.Met932Leu) c.1A>C (p.Met1Leu) c.2602A>C (p.Met868Leu) | |
1 | g.209618567T= | CA2484296295 | LAMB3 | c.2794A= (p.Met932=) c.1A= (p.Met1=) c.2602A= (p.Met868=) | |
1 | g.209618568C>A | CA344585185 | LAMB3 | c.2793G>T (p.Lys931Asn) c.-1G>T (n.-1G>T) c.2601G>T (p.Lys867Asn) | |
1 | g.209618568C= | CA2484296296 | LAMB3 | c.2793G= (p.Lys931=) c.-1G= (n.-1G=) c.2601G= (p.Lys867=) | |
1 | g.209618568C>G | CA344585186 | LAMB3 | c.2793G>C (p.Lys931Asn) c.-1G>C (n.-1G>C) c.2601G>C (p.Lys867Asn) | |
1 | g.209618568C>T | CA423030098 | LAMB3 | c.2793G>A (p.Lys931=) c.-1G>A (n.-1G>A) c.2601G>A (p.Lys867=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.209618569T>A | CA344585187 | LAMB3 | c.2792A>T (p.Lys931Met) c.-2A>T (n.-2A>T) c.2600A>T (p.Lys867Met) | |
1 | g.209618569T>C | CA344585188 | LAMB3 | c.2792A>G (p.Lys931Arg) c.-2A>G (n.-2A>G) c.2600A>G (p.Lys867Arg) | |
1 | g.209618569T>G | CA344585189 | LAMB3 | c.2792A>C (p.Lys931Thr) c.-2A>C (n.-2A>C) c.2600A>C (p.Lys867Thr) | |
1 | g.209618570T>A | CA344585190 | LAMB3 | c.2791A>T (p.Lys931Ter) c.-3A>T (n.-3A>T) c.2599A>T (p.Lys867Ter) | |
1 | g.209618570T>C | CA344585191 | LAMB3 | c.2791A>G (p.Lys931Glu) c.-3A>G (n.-3A>G) c.2599A>G (p.Lys867Glu) | dbSNP |
1 | g.209618570T>G | CA344585192 | LAMB3 | c.2791A>C (p.Lys931Gln) c.-3A>C (n.-3A>C) c.2599A>C (p.Lys867Gln) | |
1 | g.209618570T= | CA2484296297 | LAMB3 | c.2791A= (p.Lys931=) c.-3A= (n.-3A=) c.2599A= (p.Lys867=) | |
1 | g.209618571C>A | CA344585193 | LAMB3 | c.2790G>T (p.Gln930His) c.-4G>T (n.-4G>T) c.2598G>T (p.Gln866His) | |
1 | g.209618571C= | CA2484296298 | LAMB3 | c.2790G= (p.Gln930=) c.-4G= (n.-4G=) c.2598G= (p.Gln866=) | |
1 | g.209618571C>G | CA344585194 | LAMB3 | c.2790G>C (p.Gln930His) c.-4G>C (n.-4G>C) c.2598G>C (p.Gln866His) | |
1 | g.209618571C>T | CA1375095 | LAMB3 | c.2790G>A (p.Gln930=) c.-4G>A (n.-4G>A) c.2598G>A (p.Gln866=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209618572T>A | CA344585195 | LAMB3 | c.2789A>T (p.Gln930Leu) c.-5A>T (n.-5A>T) c.2597A>T (p.Gln866Leu) | |
1 | g.209618572T>C | CA344585196 | LAMB3 | c.2789A>G (p.Gln930Arg) c.-5A>G (n.-5A>G) c.2597A>G (p.Gln866Arg) | COSMIC |
1 | g.209618572T>G | CA344585197 | LAMB3 | c.2789A>C (p.Gln930Pro) c.-5A>C (n.-5A>C) c.2597A>C (p.Gln866Pro) | dbSNP |
1 | g.209618572T= | CA2484296299 | LAMB3 | c.2789A= (p.Gln930=) c.-5A= (n.-5A=) c.2597A= (p.Gln866=) | |
1 | g.209618573G>A | CA344585198 | LAMB3 | c.2788C>T (p.Gln930Ter) c.-6C>T (n.-6C>T) c.2596C>T (p.Gln866Ter) | ClinVar dbSNP gnomAD v4 |
1 | g.209618573G>C | CA344585199 | LAMB3 | c.2788C>G (p.Gln930Glu) c.-6C>G (n.-6C>G) c.2596C>G (p.Gln866Glu) | |
1 | g.209618573G>T | CA344585200 | LAMB3 | c.2788C>A (p.Gln930Lys) c.-6C>A (n.-6C>A) c.2596C>A (p.Gln866Lys) | COSMIC |
1 | g.209618574C>A | CA423030108 | LAMB3 | c.2787G>T (p.Leu929=) c.-7G>T (n.-7G>T) c.2595G>T (p.Leu865=) | |
1 | g.209618574C>G | CA423030109 | LAMB3 | c.2787G>C (p.Leu929=) c.-7G>C (n.-7G>C) c.2595G>C (p.Leu865=) | |
1 | g.209618574C>T | CA423030110 | LAMB3 | c.2787G>A (p.Leu929=) c.-7G>A (n.-7G>A) c.2595G>A (p.Leu865=) | gnomAD v4 |
1 | g.209618575A>C | CA344585201 | LAMB3 | c.2786T>G (p.Leu929Arg) c.-8T>G (n.-8T>G) c.2594T>G (p.Leu865Arg) | |
1 | g.209618575A>G | CA344585203 | LAMB3 | c.2786T>C (p.Leu929Pro) c.-8T>C (n.-8T>C) c.2594T>C (p.Leu865Pro) | |
1 | g.209618575A>T | CA344585202 | LAMB3 | c.2786T>A (p.Leu929Gln) c.-8T>A (n.-8T>A) c.2594T>A (p.Leu865Gln) | |
1 | g.209618576G>A | CA423030114 | LAMB3 | c.2785C>T (p.Leu929=) c.-9C>T (n.-9C>T) c.2593C>T (p.Leu865=) | ClinVar dbSNP |
1 | g.209618576G>C | CA344585204 | LAMB3 | c.2785C>G (p.Leu929Val) c.-9C>G (n.-9C>G) c.2593C>G (p.Leu865Val) | |
1 | g.209618576G>T | CA344585205 | LAMB3 | c.2785C>A (p.Leu929Met) c.-9C>A (n.-9C>A) c.2593C>A (p.Leu865Met) | |
1 | g.209618577A>C | CA423030115 | LAMB3 | c.2784T>G (p.Val928=) c.-10T>G (n.-10T>G) c.2592T>G (p.Val864=) | |
1 | g.209618577A>G | CA423030116 | LAMB3 | c.2784T>C (p.Val928=) c.-10T>C (n.-10T>C) c.2592T>C (p.Val864=) | |
1 | g.209618577A>T | CA423030117 | LAMB3 | c.2784T>A (p.Val928=) c.-10T>A (n.-10T>A) c.2592T>A (p.Val864=) | |
1 | g.209618578A>C | CA344585206 | LAMB3 | c.2783T>G (p.Val928Gly) c.-11T>G (n.-11T>G) c.2591T>G (p.Val864Gly) | |
1 | g.209618578A>G | CA344585207 | LAMB3 | c.2783T>C (p.Val928Ala) c.-11T>C (n.-11T>C) c.2591T>C (p.Val864Ala) | gnomAD v4 |
1 | g.209618578A>T | CA344585208 | LAMB3 | c.2783T>A (p.Val928Asp) c.-11T>A (n.-11T>A) c.2591T>A (p.Val864Asp) | |
1 | g.209618579C>A | CA344585210 | LAMB3 | c.2782G>T (p.Val928Phe) c.-12G>T (n.-12G>T) c.2590G>T (p.Val864Phe) | |
1 | g.209618579C= | CA2484296300 | LAMB3 | c.2782G= (p.Val928=) c.-12G= (n.-12G=) c.2590G= (p.Val864=) | |
1 | g.209618579C>G | CA344585211 | LAMB3 | c.2782G>C (p.Val928Leu) c.-12G>C (n.-12G>C) c.2590G>C (p.Val864Leu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209618579C>T | CA344585209 | LAMB3 | c.2782G>A (p.Val928Ile) c.-12G>A (n.-12G>A) c.2590G>A (p.Val864Ile) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.209618580A= | CA2484296301 | LAMB3 | c.2781T= (p.Thr927=) c.-13T= (n.-13T=) c.2589T= (p.Thr863=) | |
1 | g.209618580A>C | CA36750229 | LAMB3 | c.2781T>G (p.Thr927=) c.-13T>G (n.-13T>G) c.2589T>G (p.Thr863=) | dbSNP |
1 | g.209618580A>G | CA423030120 | LAMB3 | c.2781T>C (p.Thr927=) c.-13T>C (n.-13T>C) c.2589T>C (p.Thr863=) | |
1 | g.209618580A>T | CA423030121 | LAMB3 | c.2781T>A (p.Thr927=) c.-13T>A (n.-13T>A) c.2589T>A (p.Thr863=) | |
1 | g.209618581G>A | CA344585212 | LAMB3 | c.2780C>T (p.Thr927Ile) c.-14C>T (n.-14C>T) c.2588C>T (p.Thr863Ile) | |
1 | g.209618581G>C | CA344585213 | LAMB3 | c.2780C>G (p.Thr927Ser) c.-14C>G (n.-14C>G) c.2588C>G (p.Thr863Ser) | |
1 | g.209618581G>T | CA344585214 | LAMB3 | c.2780C>A (p.Thr927Asn) c.-14C>A (n.-14C>A) c.2588C>A (p.Thr863Asn) | |
1 | g.209618582T>A | CA344585215 | LAMB3 | c.2779A>T (p.Thr927Ser) c.-15A>T (n.-15A>T) c.2587A>T (p.Thr863Ser) | |
1 | g.209618582T>C | CA1375096 | LAMB3 | c.2779A>G (p.Thr927Ala) c.-15A>G (n.-15A>G) c.2587A>G (p.Thr863Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209618582T>G | CA344585216 | LAMB3 | c.2779A>C (p.Thr927Pro) c.-15A>C (n.-15A>C) c.2587A>C (p.Thr863Pro) | |
1 | g.209618582T= | CA2484296302 | LAMB3 | c.2779A= (p.Thr927=) c.-15A= (n.-15A=) c.2587A= (p.Thr863=) | |
1 | g.209618583A>C | CA423030123 | LAMB3 | c.2778T>G (p.Ala926=) c.-16T>G (n.-16T>G) c.2586T>G (p.Ala862=) | |
1 | g.209618583A>G | CA423030124 | LAMB3 | c.2778T>C (p.Ala926=) c.-16T>C (n.-16T>C) c.2586T>C (p.Ala862=) | ClinVar |
1 | g.209618583A>T | CA423030125 | LAMB3 | c.2778T>A (p.Ala926=) c.-16T>A (n.-16T>A) c.2586T>A (p.Ala862=) | |
1 | g.209618584G>A | CA344585218 | LAMB3 | c.2777C>T (p.Ala926Val) c.-17C>T (n.-17C>T) c.2585C>T (p.Ala862Val) | |
1 | g.209618584G>C | CA344585217 | LAMB3 | c.2777C>G (p.Ala926Gly) c.-17C>G (n.-17C>G) c.2585C>G (p.Ala862Gly) | ClinVar dbSNP |
1 | g.209618584G= | CA1139912083 | LAMB3 | c.2777C= (p.Ala926=) c.-17C= (n.-17C=) c.2585C= (p.Ala862=) | |
1 | g.209618584G>T | CA1375097 | LAMB3 | c.2777C>A (p.Ala926Asp) c.-17C>A (n.-17C>A) c.2585C>A (p.Ala862Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618585C>A | CA344585219 | LAMB3 | c.2776G>T (p.Ala926Ser) c.-18G>T (n.-18G>T) c.2584G>T (p.Ala862Ser) | |
1 | g.209618585C>G | CA344585220 | LAMB3 | c.2776G>C (p.Ala926Pro) c.-18G>C (n.-18G>C) c.2584G>C (p.Ala862Pro) | |
1 | g.209618585C>T | CA344585221 | LAMB3 | c.2776G>A (p.Ala926Thr) c.-18G>A (n.-18G>A) c.2584G>A (p.Ala862Thr) | |
1 | g.209618586T>A | CA423030127 | LAMB3 | c.2775A>T (p.Ser925=) c.-19A>T (n.-19A>T) c.2583A>T (p.Ser861=) | |
1 | g.209618586T>C | CA423030128 | LAMB3 | c.2775A>G (p.Ser925=) c.-19A>G (n.-19A>G) c.2583A>G (p.Ser861=) | |
1 | g.209618586T>G | CA423030130 | LAMB3 | c.2775A>C (p.Ser925=) c.-19A>C (n.-19A>C) c.2583A>C (p.Ser861=) | |
1 | g.209618587G>A | CA36750234 | LAMB3 | c.2774C>T (p.Ser925Leu) c.-20C>T (n.-20C>T) c.2582C>T (p.Ser861Leu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209618587G>C | CA344585222 | LAMB3 | c.2774C>G (p.Ser925Ter) c.-20C>G (n.-20C>G) c.2582C>G (p.Ser861Ter) | |
1 | g.209618587G= | CA1147672332 | LAMB3 | c.2774C= (p.Ser925=) c.-20C= (n.-20C=) c.2582C= (p.Ser861=) | |
1 | g.209618587G>T | CA344585223 | LAMB3 | c.2774C>A (p.Ser925Ter) c.-20C>A (n.-20C>A) c.2582C>A (p.Ser861Ter) | |
1 | g.209618588_209618589del | CA2580061994 | LAMB3 | c.2773_2774del (p.Ala926TyrfsTer8) c.-21_-20del (n.-21_-20del) c.2581_2582del (p.Ala862TyrfsTer8) | ClinVar |
1 | g.209618588A>C | CA344585224 | LAMB3 | c.2773T>G (p.Ser925Ala) c.-21T>G (n.-21T>G) c.2581T>G (p.Ser861Ala) | gnomAD v4 |
1 | g.209618588A>G | CA344585226 | LAMB3 | c.2773T>C (p.Ser925Pro) c.-21T>C (n.-21T>C) c.2581T>C (p.Ser861Pro) | |
1 | g.209618588A>T | CA344585225 | LAMB3 | c.2773T>A (p.Ser925Thr) c.-21T>A (n.-21T>A) c.2581T>A (p.Ser861Thr) | |
1 | g.209618589G>A | CA423030134 | LAMB3 | c.2772C>T (p.Asp924=) c.-22C>T (n.-22C>T) c.2580C>T (p.Asp860=) | ClinVar dbSNP |
1 | g.209618589G>C | CA344585227 | LAMB3 | c.2772C>G (p.Asp924Glu) c.-22C>G (n.-22C>G) c.2580C>G (p.Asp860Glu) | |
1 | g.209618589G>T | CA344585228 | LAMB3 | c.2772C>A (p.Asp924Glu) c.-22C>A (n.-22C>A) c.2580C>A (p.Asp860Glu) | |
1 | g.209618590T>A | CA344585229 | LAMB3 | c.2771A>T (p.Asp924Val) c.-23A>T (n.-23A>T) c.2579A>T (p.Asp860Val) | dbSNP |
1 | g.209618590T>C | CA344585230 | LAMB3 | c.2771A>G (p.Asp924Gly) c.-23A>G (n.-23A>G) c.2579A>G (p.Asp860Gly) | |
1 | g.209618590T>G | CA344585231 | LAMB3 | c.2771A>C (p.Asp924Ala) c.-23A>C (n.-23A>C) c.2579A>C (p.Asp860Ala) | gnomAD v4 |
1 | g.209618590T= | CA2484296303 | LAMB3 | c.2771A= (p.Asp924=) c.-23A= (n.-23A=) c.2579A= (p.Asp860=) | |
1 | g.209618591C>A | CA344585232 | LAMB3 | c.2770G>T (p.Asp924Tyr) c.-24G>T (n.-24G>T) c.2578G>T (p.Asp860Tyr) | |
1 | g.209618591C= | CA2484296304 | LAMB3 | c.2770G= (p.Asp924=) c.-24G= (n.-24G=) c.2578G= (p.Asp860=) | |
1 | g.209618591C>G | CA344585233 | LAMB3 | c.2770G>C (p.Asp924His) c.-24G>C (n.-24G>C) c.2578G>C (p.Asp860His) | |
1 | g.209618591C>T | CA344585234 | LAMB3 | c.2770G>A (p.Asp924Asn) c.-24G>A (n.-24G>A) c.2578G>A (p.Asp860Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209618591_209618593delinsCTG | CA2484296305 | LAMB3 | c.2768_2770delinsCAG (p.Thr923=) c.-26_-24delinsCAG (n.-26_-24delinsCAG) c.2576_2578delinsCAG (p.Thr859=) | |
1 | g.209618592T>A | CA423030137 | LAMB3 | c.2769A>T (p.Thr923=) c.-25A>T (n.-25A>T) c.2577A>T (p.Thr859=) | |
1 | g.209618592T>C | CA423030138 | LAMB3 | c.2769A>G (p.Thr923=) c.-25A>G (n.-25A>G) c.2577A>G (p.Thr859=) | |
1 | g.209618592T>G | CA423030139 | LAMB3 | c.2769A>C (p.Thr923=) c.-25A>C (n.-25A>C) c.2577A>C (p.Thr859=) | |
1 | g.209618594_209618595del | CA913189882 | LAMB3 | c.2768_2769del (p.Thr923ArgfsTer11) c.-26_-25del (n.-26_-25del) c.2576_2577del (p.Thr859ArgfsTer11) | ClinVar dbSNP |
1 | g.209618593G>A | CA344585235 | LAMB3 | c.2768C>T (p.Thr923Ile) c.-26C>T (n.-26C>T) c.2576C>T (p.Thr859Ile) | |
1 | g.209618593G>C | CA344585236 | LAMB3 | c.2768C>G (p.Thr923Arg) c.-26C>G (n.-26C>G) c.2576C>G (p.Thr859Arg) | |
1 | g.209618593G>T | CA344585237 | LAMB3 | c.2768C>A (p.Thr923Lys) c.-26C>A (n.-26C>A) c.2576C>A (p.Thr859Lys) | |
1 | g.209618594T>A | CA344585238 | LAMB3 | c.2767A>T (p.Thr923Ser) c.-27A>T (n.-27A>T) c.2575A>T (p.Thr859Ser) | |
1 | g.209618594T>C | CA344585240 | LAMB3 | c.2767A>G (p.Thr923Ala) c.-27A>G (n.-27A>G) c.2575A>G (p.Thr859Ala) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
1 | g.209618594T>G | CA344585239 | LAMB3 | c.2767A>C (p.Thr923Pro) c.-27A>C (n.-27A>C) c.2575A>C (p.Thr859Pro) | dbSNP |
1 | g.209618594T= | CA2484296306 | LAMB3 | c.2767A= (p.Thr923=) c.-27A= (n.-27A=) c.2575A= (p.Thr859=) | |
1 | g.209618595G>A | CA423030143 | LAMB3 | c.2766C>T (p.Pro922=) c.-28C>T (n.-28C>T) c.2574C>T (p.Pro858=) | |
1 | g.209618595G>C | CA423030144 | LAMB3 | c.2766C>G (p.Pro922=) c.-28C>G (n.-28C>G) c.2574C>G (p.Pro858=) | |
1 | g.209618595G>T | CA423030145 | LAMB3 | c.2766C>A (p.Pro922=) c.-28C>A (n.-28C>A) c.2574C>A (p.Pro858=) | |
1 | g.209618596_209618688del | CA2586967985 | LAMB3 | c.2702-28_2766del c.-120_-28del (n.-120_-28del) c.2510-28_2574del | |
1 | g.209618596G>A | CA344585241 | LAMB3 | c.2765C>T (p.Pro922Leu) c.-29C>T (n.-29C>T) c.2573C>T (p.Pro858Leu) | |
1 | g.209618596G>C | CA344585242 | LAMB3 | c.2765C>G (p.Pro922Arg) c.-29C>G (n.-29C>G) c.2573C>G (p.Pro858Arg) | |
1 | g.209618596G>T | CA344585243 | LAMB3 | c.2765C>A (p.Pro922His) c.-29C>A (n.-29C>A) c.2573C>A (p.Pro858His) | |
1 | g.209618597G>A | CA344585244 | LAMB3 | c.2764C>T (p.Pro922Ser) c.-30C>T (n.-30C>T) c.2572C>T (p.Pro858Ser) | gnomAD v4 |
1 | g.209618597G>C | CA1375098 | LAMB3 | c.2764C>G (p.Pro922Ala) c.-30C>G (n.-30C>G) c.2572C>G (p.Pro858Ala) | dbSNP ExAC gnomAD v2 |
1 | g.209618597G= | CA2484296307 | LAMB3 | c.2764C= (p.Pro922=) c.-30C= (n.-30C=) c.2572C= (p.Pro858=) | |
1 | g.209618597G>T | CA344585245 | LAMB3 | c.2764C>A (p.Pro922Thr) c.-30C>A (n.-30C>A) c.2572C>A (p.Pro858Thr) | |
1 | g.209618598C>A | CA423030148 | LAMB3 | c.2763G>T (p.Leu921=) c.-31G>T (n.-31G>T) c.2571G>T (p.Leu857=) | |
1 | g.209618598C>G | CA423030149 | LAMB3 | c.2763G>C (p.Leu921=) c.-31G>C (n.-31G>C) c.2571G>C (p.Leu857=) | |
1 | g.209618598C>T | CA423030150 | LAMB3 | c.2763G>A (p.Leu921=) c.-31G>A (n.-31G>A) c.2571G>A (p.Leu857=) | ClinVar dbSNP gnomAD v4 |
1 | g.209618599A>C | CA344585246 | LAMB3 | c.2762T>G (p.Leu921Arg) c.-32T>G (n.-32T>G) c.2570T>G (p.Leu857Arg) | |
1 | g.209618599A>G | CA344585247 | LAMB3 | c.2762T>C (p.Leu921Pro) c.-32T>C (n.-32T>C) c.2570T>C (p.Leu857Pro) | |
1 | g.209618599A>T | CA344585248 | LAMB3 | c.2762T>A (p.Leu921Gln) c.-32T>A (n.-32T>A) c.2570T>A (p.Leu857Gln) | |
1 | g.209618600G>A | CA423030153 | LAMB3 | c.2761C>T (p.Leu921=) c.-33C>T (n.-33C>T) c.2569C>T (p.Leu857=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.209618600G>C | CA344585249 | LAMB3 | c.2761C>G (p.Leu921Val) c.-33C>G (n.-33C>G) c.2569C>G (p.Leu857Val) | |
1 | g.209618600G= | CA1145159424 | LAMB3 | c.2761C= (p.Leu921=) c.-33C= (n.-33C=) c.2569C= (p.Leu857=) | |
1 | g.209618600G>T | CA1375099 | LAMB3 | c.2761C>A (p.Leu921Met) c.-33C>A (n.-33C>A) c.2569C>A (p.Leu857Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |