Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.7116773dup | CA657053967 | INSR | c.*288dup (n.*288dup) | gnomAD v4 COSMIC |
19 | g.7116773del | CA10652863 | INSR | c.*288del (n.*288del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
19 | g.7116772_7116773del | CA920049235 | INSR | c.*287_*288del (n.*287_*288del) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7116771_7116773del | CA2587920721 | INSR | c.*286_*288del (n.*286_*288del) | gnomAD v4 |
19 | g.7116771G>A | CA2587920726 | INSR | c.*285C>T (n.*285C>T) | dbSNP gnomAD v4 |
19 | g.7116771G>T | CA2587920727 | INSR | c.*285C>A (n.*285C>A) | gnomAD v4 |
19 | g.7116772G>T | CA2587920728 | INSR | c.*284C>A (n.*284C>A) | gnomAD v4 |
19 | g.7116773G>A | CA2587920730 | INSR | c.*283C>T (n.*283C>T) | gnomAD v4 |
19 | g.7116773G>C | CA304865931 | INSR | c.*283C>G (n.*283C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7116773G= | CA2320763651 | INSR | c.*283C= (n.*283C=) | |
19 | g.7116773G>T | CA2587920729 | INSR | c.*283C>A (n.*283C>A) | gnomAD v4 |
19 | g.7116773_7116774delinsGA | CA2320763652 | INSR | c.*282_*283delinsTC (n.*282_*283delinsTC) | |
19 | g.7116774A= | CA2320763654 | INSR | c.*282T= (n.*282T=) | |
19 | g.7116774A>C | CA2587920731 | INSR | c.*282T>G (n.*282T>G) | gnomAD v4 |
19 | g.7116774A>G | CA2320763653 | INSR | c.*282T>C (n.*282T>C) | dbSNP gnomAD v4 |
19 | g.7116775del | CA884174873 | INSR | c.*282del (n.*282del) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7116775A>C | CA2587920732 | INSR | c.*281T>G (n.*281T>G) | gnomAD v4 |
19 | g.7116775A>G | CA2587920733 | INSR | c.*281T>C (n.*281T>C) | gnomAD v4 |
19 | g.7116776C>A | CA2320763656 | INSR | c.*280G>T (n.*280G>T) | dbSNP gnomAD v4 |
19 | g.7116776C= | CA2320763655 | INSR | c.*280G= (n.*280G=) | |
19 | g.7116776C>G | CA2587920734 | INSR | c.*280G>C (n.*280G>C) | gnomAD v4 |
19 | g.7116776C>T | CA10643413 | INSR | c.*280G>A (n.*280G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.7116777G>A | CA2320763658 | INSR | c.*279C>T (n.*279C>T) | dbSNP gnomAD v4 |
19 | g.7116777G>C | CA2587920735 | INSR | c.*279C>G (n.*279C>G) | gnomAD v4 |
19 | g.7116777G= | CA2320763657 | INSR | c.*279C= (n.*279C=) | |
19 | g.7116777G>T | CA2587920736 | INSR | c.*279C>A (n.*279C>A) | gnomAD v4 |
19 | g.7116778A= | CA2320763659 | INSR | c.*278T= (n.*278T=) | |
19 | g.7116778A>T | CA304865940 | INSR | c.*278T>A (n.*278T>A) | dbSNP gnomAD v4 |
19 | g.7116783dup | CA631692390 | INSR | c.*278dup (n.*278dup) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7116783del | CA2587920737 | INSR | c.*278del (n.*278del) | gnomAD v4 |
19 | g.7116779A>C | CA2587920738 | INSR | c.*277T>G (n.*277T>G) | gnomAD v4 |
19 | g.7116779A>G | CA2587920739 | INSR | c.*277T>C (n.*277T>C) | gnomAD v4 |
19 | g.7116781A>G | CA2587920740 | INSR | c.*275T>C (n.*275T>C) | gnomAD v4 |
19 | g.7116782A= | CA2320763661 | INSR | c.*274T= (n.*274T=) | |
19 | g.7116782A>C | CA304865944 | INSR | c.*274T>G (n.*274T>G) | dbSNP |
19 | g.7116782A>T | CA2587920741 | INSR | c.*274T>A (n.*274T>A) | gnomAD v4 |
19 | g.7116782_7116784delinsAAC | CA2320763660 | INSR | c.*272_*274delinsGTT (n.*272_*274delinsGTT) | |
19 | g.7116784_7116865del | CA993113649 | INSR | c.*193_*274del (n.*193_*274del) | gnomAD v3 gnomAD v4 |
19 | g.7116783A>C | CA2587920742 | INSR | c.*273T>G (n.*273T>G) | gnomAD v4 |
19 | g.7116783A>T | CA2587920743 | INSR | c.*273T>A (n.*273T>A) | gnomAD v4 |
19 | g.7116786_7116787del | CA2320763662 | INSR | c.*272_*273del (n.*272_*273del) | dbSNP |
19 | g.7116784C>A | CA2587920744 | INSR | c.*272G>T (n.*272G>T) | gnomAD v4 |
19 | g.7116784C>G | CA2587920745 | INSR | c.*272G>C (n.*272G>C) | gnomAD v4 |
19 | g.7116784C>T | CA2587920746 | INSR | c.*272G>A (n.*272G>A) | gnomAD v4 |
19 | g.7116785A>C | CA2587920747 | INSR | c.*271T>G (n.*271T>G) | gnomAD v4 |
19 | g.7116785A>G | CA2587920748 | INSR | c.*271T>C (n.*271T>C) | gnomAD v4 |
19 | g.7116786C>A | CA2587920749 | INSR | c.*270G>T (n.*270G>T) | gnomAD v4 |
19 | g.7116786C= | CA2320763663 | INSR | c.*270G= (n.*270G=) | |
19 | g.7116786C>G | CA2735386318 | INSR | c.*270G>C (n.*270G>C) | dbSNP |
19 | g.7116786C>T | CA993113653 | INSR | c.*270G>A (n.*270G>A) | dbSNP gnomAD v3 gnomAD v4 |