Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.53057193_53057201del | CA2756287204 | c.318-9959_318-9951del c.465-13944_465-13936del c.447+20490_447+20498del | ||
3 | g.53057193C= | CA1365145703 | c.318-9954G= c.465-13939G= c.447+20495G= | ||
3 | g.53057193C>T | CA542918799 | c.318-9954G>A c.465-13939G>A c.447+20495G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
3 | g.53057194A= | CA1365145704 | c.318-9955T= c.465-13940T= c.447+20494T= | ||
3 | g.53057194A>C | CA74805332 | c.318-9955T>G c.465-13940T>G c.447+20494T>G | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057194A>G | CA2597569095 | c.318-9955T>C c.465-13940T>C c.447+20494T>C | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057194A>T | CA542918800 | c.318-9955T>A c.465-13940T>A c.447+20494T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
3 | g.53057196_53057201delinsTGGCCA | CA1365145705 | c.318-9962_318-9957delinsTGGCCA c.465-13947_465-13942delinsTGGCCA c.447+20487_447+20492delinsTGGCCA | ||
3 | g.53057197G>A | CA2553146142 | c.318-9958C>T c.465-13943C>T c.447+20491C>T | ||
3 | g.53057200_53057204del | CA74805333 | c.318-9962_318-9958del c.465-13947_465-13943del c.447+20487_447+20491del | dbSNP | |
3 | g.53057198G>A | CA74805336 | c.318-9959C>T c.465-13944C>T c.447+20490C>T | dbSNP | |
3 | g.53057198G= | CA1365145706 | c.318-9959C= c.465-13944C= c.447+20490C= | ||
3 | g.53057200C>A | CA2597569096 | c.318-9961G>T c.465-13946G>T c.447+20488G>T | gnomAD v3 gnomAD v4 | |
3 | g.53057200C>T | CA2597569097 | c.318-9961G>A c.465-13946G>A c.447+20488G>A | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057201A= | CA1365145707 | c.318-9962T= c.465-13947T= c.447+20487T= | ||
3 | g.53057201A>G | CA1365145708 | c.318-9962T>C c.465-13947T>C c.447+20487T>C | dbSNP | |
3 | g.53057202G>A | CA1048013732 | c.318-9963C>T c.465-13948C>T c.447+20486C>T | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057202G>C | CA908188484 | c.318-9963C>G c.465-13948C>G c.447+20486C>G | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057202G= | CA1365145709 | c.318-9963C= c.465-13948C= c.447+20486C= | ||
3 | g.53057205T>G | CA74805337 | c.318-9966A>C c.465-13951A>C c.447+20483A>C | dbSNP gnomAD v2 | |
3 | g.53057205T= | CA1365145710 | c.318-9966A= c.465-13951A= c.447+20483A= | ||
3 | g.53057206G>C | CA2597569098 | c.318-9967C>G c.465-13952C>G c.447+20482C>G | gnomAD v3 gnomAD v4 | |
3 | g.53057207G>A | CA908188487 | c.318-9968C>T c.465-13953C>T c.447+20481C>T | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057207G= | CA1365145711 | c.318-9968C= c.465-13953C= c.447+20481C= | ||
3 | g.53057208T>G | CA1365145713 | c.318-9969A>C c.465-13954A>C c.447+20480A>C | dbSNP | |
3 | g.53057208T= | CA1365145712 | c.318-9969A= c.465-13954A= c.447+20480A= | ||
3 | g.53057212G>A | CA1365145715 | c.318-9973C>T c.465-13958C>T c.447+20476C>T | dbSNP | |
3 | g.53057212G= | CA1365145714 | c.318-9973C= c.465-13958C= c.447+20476C= | ||
3 | g.53057214A= | CA1365145716 | c.318-9975T= c.465-13960T= c.447+20474T= | ||
3 | g.53057214A>G | CA908188488 | c.318-9975T>C c.465-13960T>C c.447+20474T>C | dbSNP | |
3 | g.53057215C>A | CA542918801 | c.318-9976G>T c.465-13961G>T c.447+20473G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
3 | g.53057215C= | CA1365145717 | c.318-9976G= c.465-13961G= c.447+20473G= | ||
3 | g.53057218C>A | CA1365145719 | c.318-9979G>T c.465-13964G>T c.447+20470G>T | dbSNP | |
3 | g.53057218C= | CA1365145718 | c.318-9979G= c.465-13964G= c.447+20470G= | ||
3 | g.53057228G>A | CA908188490 | c.318-9989C>T c.465-13974C>T c.447+20460C>T | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057228G= | CA1365145720 | c.318-9989C= c.465-13974C= c.447+20460C= | ||
3 | g.53057229T>G | CA1365145722 | c.318-9990A>C c.465-13975A>C c.447+20459A>C | dbSNP | |
3 | g.53057229T= | CA1365145721 | c.318-9990A= c.465-13975A= c.447+20459A= | ||
3 | g.53057231A= | CA1365145723 | c.318-9992T= c.465-13977T= c.447+20457T= | ||
3 | g.53057231A>C | CA74805338 | c.318-9992T>G c.465-13977T>G c.447+20457T>G | dbSNP | |
3 | g.53057232T>A | CA908188501 | c.318-9993A>T c.465-13978A>T c.447+20456A>T | dbSNP | |
3 | g.53057232T= | CA1365145724 | c.318-9993A= c.465-13978A= c.447+20456A= | ||
3 | g.53057234C>A | CA542918802 | c.318-9995G>T c.465-13980G>T c.447+20454G>T | dbSNP gnomAD v2 | |
3 | g.53057234C= | CA1365145725 | c.318-9995G= c.465-13980G= c.447+20454G= | ||
3 | g.53057234C>T | CA1365145726 | c.318-9995G>A c.465-13980G>A c.447+20454G>A | dbSNP | |
3 | g.53057235A= | CA1365145727 | c.318-9996T= c.465-13981T= c.447+20453T= | ||
3 | g.53057235A>C | CA1365145728 | c.318-9996T>G c.465-13981T>G c.447+20453T>G | dbSNP | |
3 | g.53057235A>G | CA1048013737 | c.318-9996T>C c.465-13981T>C c.447+20453T>C | dbSNP gnomAD v3 gnomAD v4 | |
3 | g.53057236C= | CA1365145729 | c.318-9997G= c.465-13982G= c.447+20452G= | ||
3 | g.53057236C>G | CA1365145730 | c.318-9997G>C c.465-13982G>C c.447+20452G>C | dbSNP |