Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154030255_154037279delinsCACAAAGTG | CA274580 | MECP2 | c.27-4722_*112delinsCACTTTGTG c.63-4722_*112delinsCACTTTGTG c.27-4722_*39delinsCACTTTGTG c.27-4722_*945delinsCACTTTGTG c.-253-4722_*112delinsCACTTTGTG c.-254+2513_*112delinsCACTTTGTG c.-535+2513_*112delinsCACTTTGTG c.-534-4722_*112delinsCACTTTGTG | ClinVar |
X | g.154030587_154034485del | CA1139667874 | MECP2 | c.27-1928_1241del c.63-1928_1277del c.27-1928_*613del c.-253-1928_962del c.-534-1928_572del | ClinVar |
X | g.154030593_154038357del | CA2499226465 | MECP2 | c.27-5800_1235del c.63-5800_1271del c.27-5800_*607del c.-253-5800_956del c.-254+1435_956del c.-535+1435_566del c.-534-5800_566del | ClinVar |
X | g.154030623_154032653del | CA274584 | MECP2 | c.27-94_1207del c.63-94_1243del c.63-94_*579del c.27-94_*579del c.-253-94_928del c.-534-94_538del | ClinVar |
X | g.154030638_154038772del | CA274583 | MECP2 | c.27-6214_1191del c.63-6214_1227del c.63-6214_*563del c.27-6214_*563del c.-253-6214_912del c.-254+1021_912del c.-535+1021_522del c.-534-6214_522del | ClinVar |
X | g.154030638_154038583delinsAC | CA274582 | MECP2 | c.27-6026_1190delinsGT c.63-6026_1226delinsGT c.63-6026_*562delinsGT c.27-6026_*562delinsGT c.-253-6026_911delinsGT c.-254+1209_911delinsGT c.-535+1209_521delinsGT c.-534-6026_521delinsGT | ClinVar |
X | g.154030646_154036487del | CA274579 | MECP2 | c.27-3928_1184del c.63-3928_1220del c.63-3928_*556del c.27-3928_*556del c.-253-3928_905del c.-254+3307_905del c.-535+3307_515del c.-534-3928_515del | ClinVar |
X | g.154030663_154037047del | CA916084238 | MECP2 | c.27-4487_1168del c.63-4487_1204del c.63-4487_*540del c.27-4487_*540del c.-253-4487_889del c.-254+2748_889del c.-535+2748_499del c.-534-4487_499del | ClinVar |
X | g.154030672_154039641del | CA1139667883 | MECP2 | c.27-7080_1160del c.63-7080_1196del c.63-7080_*532del c.27-7080_*532del c.-253-7080_881del c.-254+155_881del c.-535+155_491del c.-534-7080_491del | ClinVar |
X | g.154030690_154038335del | CA915952024 | MECP2 | c.27-5778_1138del c.63-5778_1174del c.63-5778_*510del c.27-5778_*510del c.-253-5778_859del c.-254+1457_859del c.-535+1457_469del c.-534-5778_469del | ClinVar |
X | g.154030777_154032630del | CA915952026 | MECP2 | c.27-73_1051del c.63-73_1087del c.63-73_*423del c.27-73_*423del c.-253-73_772del c.-534-73_382del | ClinVar |
X | g.154030926_154038331delinsTGACATCAGTCCGGGCAC | CA274581 | MECP2 | c.27-5774_902delinsGTGCCCGGACTGATGTCA c.63-5774_938delinsGTGCCCGGACTGATGTCA c.63-5774_*274delinsGTGCCCGGACTGATGTCA c.15-5774_888delinsGTGCCCGGACTGATGTCA c.27-5774_*274delinsGTGCCCGGACTGATGTCA c.-253-5774_623delinsGTGCCCGGACTGATGTCA c.-254+1461_623delinsGTGCCCGGACTGATGTCA c.-535+1461_233delinsGTGCCCGGACTGATGTCA c.-534-5774_233delinsGTGCCCGGACTGATGTCA | ClinVar |
X | g.154031347_154035447del | CA891863116 | MECP2 | c.27-2890_481del c.63-2890_517del c.63-2890_468+49del n.2375-2890_2829del c.15-2890_469del c.27-2890_432+49del c.-253-2890_202del c.-534-2890_-129+49del | ClinVar |
X | g.154032292G>A | CA415176982 | MECP2 | c.292C>T (p.Pro98Ser) c.328C>T (p.Pro110Ser) c.*346C>T (n.*346C>T) n.2640C>T c.280C>T (p.Pro94Ser) c.13C>T (p.Pro5Ser) c.-269C>T (n.-269C>T) | |
X | g.154032292G>C | CA415176986 | MECP2 | c.292C>G (p.Pro98Ala) c.328C>G (p.Pro110Ala) c.*346C>G (n.*346C>G) n.2640C>G c.280C>G (p.Pro94Ala) c.13C>G (p.Pro5Ala) c.-269C>G (n.-269C>G) | |
X | g.154032292G>T | CA415176988 | MECP2 | c.292C>A (p.Pro98Thr) c.328C>A (p.Pro110Thr) c.*346C>A (n.*346C>A) n.2640C>A c.280C>A (p.Pro94Thr) c.13C>A (p.Pro5Thr) c.-269C>A (n.-269C>A) | |
X | g.154032293G>A | CA519705379 | MECP2 | c.291C>T (p.Asp97=) c.327C>T (p.Asp109=) c.*345C>T (n.*345C>T) n.2639C>T c.279C>T (p.Asp93=) c.12C>T (p.Asp4=) c.-270C>T (n.-270C>T) | |
X | g.154032293G>C | CA415176991 | MECP2 | c.291C>G (p.Asp97Glu) c.327C>G (p.Asp109Glu) c.*345C>G (n.*345C>G) n.2639C>G c.279C>G (p.Asp93Glu) c.12C>G (p.Asp4Glu) c.-270C>G (n.-270C>G) | |
X | g.154032293G= | CA2466571554 | MECP2 | c.291C= (p.Asp97=) c.327C= (p.Asp109=) c.*345C= (n.*345C=) n.2639C= c.279C= (p.Asp93=) c.12C= (p.Asp4=) c.-270C= (n.-270C=) | |
X | g.154032293G>T | CA270323 | MECP2 | c.291C>A (p.Asp97Glu) c.327C>A (p.Asp109Glu) c.*345C>A (n.*345C>A) n.2639C>A c.279C>A (p.Asp93Glu) c.12C>A (p.Asp4Glu) c.-270C>A (n.-270C>A) | ClinVar dbSNP |
X | g.154032294T>A | CA415176997 | MECP2 | c.290A>T (p.Asp97Val) c.326A>T (p.Asp109Val) c.*344A>T (n.*344A>T) n.2638A>T c.278A>T (p.Asp93Val) c.11A>T (p.Asp4Val) c.-271A>T (n.-271A>T) | |
X | g.154032294T>C | CA415176999 | MECP2 | c.290A>G (p.Asp97Gly) c.326A>G (p.Asp109Gly) c.*344A>G (n.*344A>G) n.2638A>G c.278A>G (p.Asp93Gly) c.11A>G (p.Asp4Gly) c.-271A>G (n.-271A>G) | |
X | g.154032294T>G | CA415177000 | MECP2 | c.290A>C (p.Asp97Ala) c.326A>C (p.Asp109Ala) c.*344A>C (n.*344A>C) n.2638A>C c.278A>C (p.Asp93Ala) c.11A>C (p.Asp4Ala) c.-271A>C (n.-271A>C) | |
X | g.154032295C>A | CA270316 | MECP2 | c.289G>T (p.Asp97Tyr) c.325G>T (p.Asp109Tyr) c.*343G>T (n.*343G>T) n.2637G>T c.277G>T (p.Asp93Tyr) c.10G>T (p.Asp4Tyr) c.-272G>T (n.-272G>T) | ClinVar dbSNP |
X | g.154032295C= | CA2466571555 | MECP2 | c.289G= (p.Asp97=) c.325G= (p.Asp109=) c.*343G= (n.*343G=) n.2637G= c.277G= (p.Asp93=) c.10G= (p.Asp4=) c.-272G= (n.-272G=) | |
X | g.154032295C>G | CA415177003 | MECP2 | c.289G>C (p.Asp97His) c.325G>C (p.Asp109His) c.*343G>C (n.*343G>C) n.2637G>C c.277G>C (p.Asp93His) c.10G>C (p.Asp4His) c.-272G>C (n.-272G>C) | |
X | g.154032295C>T | CA415177006 | MECP2 | c.289G>A (p.Asp97Asn) c.325G>A (p.Asp109Asn) c.*343G>A (n.*343G>A) n.2637G>A c.277G>A (p.Asp93Asn) c.10G>A (p.Asp4Asn) c.-272G>A (n.-272G>A) | |
X | g.154032296A>C | CA415177009 | MECP2 | c.288T>G (p.Asp96Glu) c.324T>G (p.Asp108Glu) c.*342T>G (n.*342T>G) n.2636T>G c.276T>G (p.Asp92Glu) c.9T>G (p.Asp3Glu) c.-273T>G (n.-273T>G) | gnomAD v4 |
X | g.154032296A>G | CA519705392 | MECP2 | c.288T>C (p.Asp96=) c.324T>C (p.Asp108=) c.*342T>C (n.*342T>C) n.2636T>C c.276T>C (p.Asp92=) c.9T>C (p.Asp3=) c.-273T>C (n.-273T>C) | |
X | g.154032296A>T | CA415177012 | MECP2 | c.288T>A (p.Asp96Glu) c.324T>A (p.Asp108Glu) c.*342T>A (n.*342T>A) n.2636T>A c.276T>A (p.Asp92Glu) c.9T>A (p.Asp3Glu) c.-273T>A (n.-273T>A) | |
X | g.154032297T>A | CA415177015 | MECP2 | c.287A>T (p.Asp96Val) c.323A>T (p.Asp108Val) c.*341A>T (n.*341A>T) n.2635A>T c.275A>T (p.Asp92Val) c.8A>T (p.Asp3Val) c.-274A>T (n.-274A>T) | |
X | g.154032297T>C | CA415177019 | MECP2 | c.287A>G (p.Asp96Gly) c.323A>G (p.Asp108Gly) c.*341A>G (n.*341A>G) n.2635A>G c.275A>G (p.Asp92Gly) c.8A>G (p.Asp3Gly) c.-274A>G (n.-274A>G) | |
X | g.154032297T>G | CA415177025 | MECP2 | c.287A>C (p.Asp96Ala) c.323A>C (p.Asp108Ala) c.*341A>C (n.*341A>C) n.2635A>C c.275A>C (p.Asp92Ala) c.8A>C (p.Asp3Ala) c.-274A>C (n.-274A>C) | |
X | g.154032297_154032301delinsTCATA | CA2466571556 | MECP2 | c.283_287delinsTATGA (p.Tyr95=) c.319_323delinsTATGA (p.Tyr107=) c.*337_*341delinsTATGA (n.*337_*341delinsTATGA) n.2631_2635delinsTATGA c.271_275delinsTATGA (p.Tyr91=) c.4_8delinsTATGA (p.Tyr2=) c.-278_-274delinsTATGA (n.-278_-274delinsTATGA) | |
X | g.154032298C>A | CA415177028 | MECP2 | c.286G>T (p.Asp96Tyr) c.322G>T (p.Asp108Tyr) c.*340G>T (n.*340G>T) n.2634G>T c.274G>T (p.Asp92Tyr) c.7G>T (p.Asp3Tyr) c.-275G>T (n.-275G>T) | |
X | g.154032298C>G | CA415177030 | MECP2 | c.286G>C (p.Asp96His) c.322G>C (p.Asp108His) c.*340G>C (n.*340G>C) n.2634G>C c.274G>C (p.Asp92His) c.7G>C (p.Asp3His) c.-275G>C (n.-275G>C) | gnomAD v4 |
X | g.154032298C>T | CA415177031 | MECP2 | c.286G>A (p.Asp96Asn) c.322G>A (p.Asp108Asn) c.*340G>A (n.*340G>A) n.2634G>A c.274G>A (p.Asp92Asn) c.7G>A (p.Asp3Asn) c.-275G>A (n.-275G>A) | |
X | g.154032301_154032304del | CA658824341 | MECP2 | c.283_286del (p.Tyr95MetfsTer29) c.319_322del (p.Tyr107MetfsTer29) c.*337_*340del (n.*337_*340del) n.2631_2634del c.271_274del (p.Tyr91MetfsTer29) c.4_7del (p.Tyr2MetfsTer29) c.-278_-275del (n.-278_-275del) | ClinVar dbSNP |
X | g.154032299A>C | CA415177035 | MECP2 | c.285T>G (p.Tyr95Ter) c.321T>G (p.Tyr107Ter) c.*339T>G (n.*339T>G) n.2633T>G c.273T>G (p.Tyr91Ter) c.6T>G (p.Tyr2Ter) c.-276T>G (n.-276T>G) | |
X | g.154032299A>G | CA519705406 | MECP2 | c.285T>C (p.Tyr95=) c.321T>C (p.Tyr107=) c.*339T>C (n.*339T>C) n.2633T>C c.273T>C (p.Tyr91=) c.6T>C (p.Tyr2=) c.-276T>C (n.-276T>C) | |
X | g.154032299A>T | CA415177037 | MECP2 | c.285T>A (p.Tyr95Ter) c.321T>A (p.Tyr107Ter) c.*339T>A (n.*339T>A) n.2633T>A c.273T>A (p.Tyr91Ter) c.6T>A (p.Tyr2Ter) c.-276T>A (n.-276T>A) | |
X | g.154032300T>A | CA415177040 | MECP2 | c.284A>T (p.Tyr95Phe) c.320A>T (p.Tyr107Phe) c.*338A>T (n.*338A>T) n.2632A>T c.272A>T (p.Tyr91Phe) c.5A>T (p.Tyr2Phe) c.-277A>T (n.-277A>T) | |
X | g.154032300T>C | CA415177042 | MECP2 | c.284A>G (p.Tyr95Cys) c.320A>G (p.Tyr107Cys) c.*338A>G (n.*338A>G) n.2632A>G c.272A>G (p.Tyr91Cys) c.5A>G (p.Tyr2Cys) c.-277A>G (n.-277A>G) | |
X | g.154032300T>G | CA415177045 | MECP2 | c.284A>C (p.Tyr95Ser) c.320A>C (p.Tyr107Ser) c.*338A>C (n.*338A>C) n.2632A>C c.272A>C (p.Tyr91Ser) c.5A>C (p.Tyr2Ser) c.-277A>C (n.-277A>C) | |
X | g.154032301A>C | CA415177061 | MECP2 | c.283T>G (p.Tyr95Asp) c.319T>G (p.Tyr107Asp) c.*337T>G (n.*337T>G) n.2631T>G c.271T>G (p.Tyr91Asp) c.4T>G (p.Tyr2Asp) c.-278T>G (n.-278T>G) | |
X | g.154032301A>G | CA415177064 | MECP2 | c.283T>C (p.Tyr95His) c.319T>C (p.Tyr107His) c.*337T>C (n.*337T>C) n.2631T>C c.271T>C (p.Tyr91His) c.4T>C (p.Tyr2His) c.-278T>C (n.-278T>C) | |
X | g.154032301A>T | CA415177058 | MECP2 | c.283T>A (p.Tyr95Asn) c.319T>A (p.Tyr107Asn) c.*337T>A (n.*337T>A) n.2631T>A c.271T>A (p.Tyr91Asn) c.4T>A (p.Tyr2Asn) c.-278T>A (n.-278T>A) | |
X | g.154032302C>A | CA415177068 | MECP2 | c.282G>T (p.Met94Ile) c.318G>T (p.Met106Ile) c.*336G>T (n.*336G>T) n.2630G>T c.270G>T (p.Met90Ile) c.3G>T (p.Met1Ile) c.-279G>T (n.-279G>T) | COSMIC |
X | g.154032302C>G | CA415177071 | MECP2 | c.282G>C (p.Met94Ile) c.318G>C (p.Met106Ile) c.*336G>C (n.*336G>C) n.2630G>C c.270G>C (p.Met90Ile) c.3G>C (p.Met1Ile) c.-279G>C (n.-279G>C) | |
X | g.154032302C>T | CA415177074 | MECP2 | c.282G>A (p.Met94Ile) c.318G>A (p.Met106Ile) c.*336G>A (n.*336G>A) n.2630G>A c.270G>A (p.Met90Ile) c.3G>A (p.Met1Ile) c.-279G>A (n.-279G>A) |