Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.53056868A= | CA1365145565 | c.318-9629T= c.465-13614T= c.447+20820T= | ||
3 | g.53056868A>T | CA1365145566 | c.318-9629T>A c.465-13614T>A c.447+20820T>A | dbSNP | |
3 | g.53056870T>A | CA2756287195 | c.318-9631A>T c.465-13616A>T c.447+20818A>T | ||
3 | g.53056871A>T | CA2501035004 | c.318-9632T>A c.465-13617T>A c.447+20817T>A | ||
3 | g.53056883A= | CA1365145567 | c.318-9644T= c.465-13629T= c.447+20805T= | ||
3 | g.53056883A>C | CA542918785 | c.318-9644T>G c.465-13629T>G c.447+20805T>G | dbSNP gnomAD v2 | |
3 | g.53056883A>G | CA74805228 | c.318-9644T>C c.465-13629T>C c.447+20805T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
3 | g.53056884T>C | CA1048013649 | c.318-9645A>G c.465-13630A>G c.447+20804A>G | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056884T= | CA1365145568 | c.318-9645A= c.465-13630A= c.447+20804A= | ||
3 | g.53056885G>A | CA74805233 | c.318-9646C>T c.465-13631C>T c.447+20803C>T | dbSNP | |
3 | g.53056885G= | CA1365145569 | c.318-9646C= c.465-13631C= c.447+20803C= | ||
3 | g.53056891C>A | CA2572490199 | c.318-9652G>T c.465-13637G>T c.447+20797G>T | ||
3 | g.53056891C= | CA1365145570 | c.318-9652G= c.465-13637G= c.447+20797G= | ||
3 | g.53056891C>T | CA74805239 | c.318-9652G>A c.465-13637G>A c.447+20797G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
3 | g.53056892A= | CA1365145571 | c.318-9653T= c.465-13638T= c.447+20796T= | ||
3 | g.53056892A>G | CA1365145572 | c.318-9653T>C c.465-13638T>C c.447+20796T>C | dbSNP | |
3 | g.53056893A>G | CA2502977287 | c.318-9654T>C c.465-13639T>C c.447+20795T>C | ||
3 | g.53056897C= | CA1365145573 | c.318-9658G= c.465-13643G= c.447+20791G= | ||
3 | g.53056897C>G | CA1048013651 | c.318-9658G>C c.465-13643G>C c.447+20791G>C | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056898T>C | CA2597569091 | c.318-9659A>G c.465-13644A>G c.447+20790A>G | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056904G= | CA1365145574 | c.318-9665C= c.465-13650C= c.447+20784C= | ||
3 | g.53056906_53056935dup | CA908188321 | c.318-9695_318-9666dup c.465-13680_465-13651dup c.447+20754_447+20783dup | dbSNP | |
3 | g.53056908T>G | CA1048013652 | c.318-9669A>C c.465-13654A>C c.447+20780A>C | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056908T= | CA1365145575 | c.318-9669A= c.465-13654A= c.447+20780A= | ||
3 | g.53056912T>C | CA74805242 | c.318-9673A>G c.465-13658A>G c.447+20776A>G | dbSNP | |
3 | g.53056912T= | CA1365145576 | c.318-9673A= c.465-13658A= c.447+20776A= | ||
3 | g.53056913G>A | CA542918786 | c.318-9674C>T c.465-13659C>T c.447+20775C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
3 | g.53056913G= | CA1365145577 | c.318-9674C= c.465-13659C= c.447+20775C= | ||
3 | g.53056920T>C | CA2526204360 | c.318-9681A>G c.465-13666A>G c.447+20768A>G | ||
3 | g.53056924A= | CA1365145578 | c.318-9685T= c.465-13670T= c.447+20764T= | ||
3 | g.53056924A>C | CA2756287196 | c.318-9685T>G c.465-13670T>G c.447+20764T>G | ||
3 | g.53056924A>G | CA1365145579 | c.318-9685T>C c.465-13670T>C c.447+20764T>C | dbSNP | |
3 | g.53056925G>A | CA74805256 | c.318-9686C>T c.465-13671C>T c.447+20763C>T | dbSNP | |
3 | g.53056925G= | CA1365145580 | c.318-9686C= c.465-13671C= c.447+20763C= | ||
3 | g.53056926A= | CA1365145581 | c.318-9687T= c.465-13672T= c.447+20762T= | ||
3 | g.53056926A>G | CA908188330 | c.318-9687T>C c.465-13672T>C c.447+20762T>C | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056928G>A | CA1365145582 | c.318-9689C>T c.465-13674C>T c.447+20760C>T | dbSNP | |
3 | g.53056928G= | CA1365145583 | c.318-9689C= c.465-13674C= c.447+20760C= | ||
3 | g.53056933C= | CA1365145584 | c.318-9694G= c.465-13679G= c.447+20755G= | ||
3 | g.53056933C>T | CA908188331 | c.318-9694G>A c.465-13679G>A c.447+20755G>A | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056937G>C | CA1365145586 | c.318-9698C>G c.465-13683C>G c.447+20751C>G | dbSNP | |
3 | g.53056937G= | CA1365145585 | c.318-9698C= c.465-13683C= c.447+20751C= | ||
3 | g.53056940A= | CA1365145587 | c.318-9701T= c.465-13686T= c.447+20748T= | ||
3 | g.53056940A>G | CA1365145588 | c.318-9701T>C c.465-13686T>C c.447+20748T>C | dbSNP | |
3 | g.53056944C>A | CA908188332 | c.318-9705G>T c.465-13690G>T c.447+20744G>T | dbSNP | |
3 | g.53056944C= | CA1365145589 | c.318-9705G= c.465-13690G= c.447+20744G= | ||
3 | g.53056947_53056951delinsGTGTT | CA1365145590 | c.318-9712_318-9708delinsAACAC c.465-13697_465-13693delinsAACAC c.447+20737_447+20741delinsAACAC | ||
3 | g.53056948T>C | CA1365145591 | c.318-9709A>G c.465-13694A>G c.447+20740A>G | dbSNP | |
3 | g.53056948T= | CA1365145592 | c.318-9709A= c.465-13694A= c.447+20740A= | ||
3 | g.53056954_53056957del | CA908188340 | c.318-9712_318-9709del c.465-13697_465-13694del c.447+20737_447+20740del | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056951T>G | CA1365145594 | c.318-9712A>C c.465-13697A>C c.447+20737A>C | dbSNP | |
3 | g.53056951T= | CA1365145593 | c.318-9712A= c.465-13697A= c.447+20737A= | ||
3 | g.53056955T>C | CA1048013658 | c.318-9716A>G c.465-13701A>G c.447+20733A>G | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53056955T= | CA1365145595 | c.318-9716A= c.465-13701A= c.447+20733A= | ||
3 | g.53056968C= | CA1365145596 | c.318-9729G= c.465-13714G= c.447+20720G= | ||
3 | g.53056968C>T | CA1365145597 | c.318-9729G>A c.465-13714G>A c.447+20720G>A | dbSNP |