Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.18281038_18281040delCA637153531TMPRSS15c.2668_2668+2del
c.2803_2803+2del
c.2758_2758+2del
c.2722_2722+2del
c.2713_2713+2del
gnomAD v2 gnomAD v3 gnomAD v4
21g.18281039C>ACA409847821TMPRSS15c.2668+1G>T (n.2668+1G>T)
c.2803+1G>T (n.2803+1G>T)
c.2758+1G>T (n.2758+1G>T)
c.2722+1G>T (n.2722+1G>T)
c.2713+1G>T (n.2713+1G>T)
21g.18281039C=CA2379736632TMPRSS15c.2668+1G= (n.2668+1G=)
c.2803+1G= (n.2803+1G=)
c.2758+1G= (n.2758+1G=)
c.2722+1G= (n.2722+1G=)
c.2713+1G= (n.2713+1G=)
21g.18281039C>GCA409847822TMPRSS15c.2668+1G>C (n.2668+1G>C)
c.2803+1G>C (n.2803+1G>C)
c.2758+1G>C (n.2758+1G>C)
c.2722+1G>C (n.2722+1G>C)
c.2713+1G>C (n.2713+1G>C)
21g.18281039C>TCA409847823TMPRSS15c.2668+1G>A (n.2668+1G>A)
c.2803+1G>A (n.2803+1G>A)
c.2758+1G>A (n.2758+1G>A)
c.2722+1G>A (n.2722+1G>A)
c.2713+1G>A (n.2713+1G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.18281040C>ACA409847824TMPRSS15c.2668G>T (p.Asp890Tyr)
c.2803G>T (p.Asp935Tyr)
c.2758G>T (p.Asp920Tyr)
c.2722G>T (p.Asp908Tyr)
c.2713G>T (p.Asp905Tyr)
21g.18281040C=CA2379736633TMPRSS15c.2668G= (p.Asp890=)
c.2803G= (p.Asp935=)
c.2758G= (p.Asp920=)
c.2722G= (p.Asp908=)
c.2713G= (p.Asp905=)
21g.18281040C>GCA409847825TMPRSS15c.2668G>C (p.Asp890His)
c.2803G>C (p.Asp935His)
c.2758G>C (p.Asp920His)
c.2722G>C (p.Asp908His)
c.2713G>C (p.Asp905His)
gnomAD v4
21g.18281040C>TCA9983981TMPRSS15c.2668G>A (p.Asp890Asn)
c.2803G>A (p.Asp935Asn)
c.2758G>A (p.Asp920Asn)
c.2722G>A (p.Asp908Asn)
c.2713G>A (p.Asp905Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.18281040_18281044delinsCTGTGCA2379736634TMPRSS15c.2664_2668delinsCACAG (p.Tyr888=)
c.2799_2803delinsCACAG (p.Tyr933=)
c.2754_2758delinsCACAG (p.Tyr918=)
c.2718_2722delinsCACAG (p.Tyr906=)
c.2709_2713delinsCACAG (p.Tyr903=)
21g.18281041T>ACA511459087TMPRSS15c.2667A>T (p.Thr889=)
c.2802A>T (p.Thr934=)
c.2757A>T (p.Thr919=)
c.2721A>T (p.Thr907=)
c.2712A>T (p.Thr904=)
21g.18281041T>CCA318130070TMPRSS15c.2667A>G (p.Thr889=)
c.2802A>G (p.Thr934=)
c.2757A>G (p.Thr919=)
c.2721A>G (p.Thr907=)
c.2712A>G (p.Thr904=)
dbSNP
21g.18281041T>GCA511459088TMPRSS15c.2667A>C (p.Thr889=)
c.2802A>C (p.Thr934=)
c.2757A>C (p.Thr919=)
c.2721A>C (p.Thr907=)
c.2712A>C (p.Thr904=)
21g.18281041T=CA2379736635TMPRSS15c.2667A= (p.Thr889=)
c.2802A= (p.Thr934=)
c.2757A= (p.Thr919=)
c.2721A= (p.Thr907=)
c.2712A= (p.Thr904=)
21g.18281041_18281042insTTCA637153532TMPRSS15c.2667_2668insAA (p.Asp890LysfsTer?)
c.2802_2803insAA (p.Asp935LysfsTer?)
c.2757_2758insAA (p.Asp920LysfsTer?)
c.2721_2722insAA (p.Asp908LysfsTer?)
c.2712_2713insAA (p.Asp905LysfsTer?)
gnomAD v2 gnomAD v3 gnomAD v4
21g.18281042_18281045delCA9983982TMPRSS15c.2664_2667del (p.Tyr888Ter)
c.2799_2802del (p.Tyr933Ter)
c.2754_2757del (p.Tyr918Ter)
c.2718_2721del (p.Tyr906Ter)
c.2709_2712del (p.Tyr903Ter)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.18281042delCA2577464980TMPRSS15c.2666del (p.Thr889LysfsTer?)
c.2801del (p.Thr934LysfsTer?)
c.2756del (p.Thr919LysfsTer?)
c.2720del (p.Thr907LysfsTer?)
c.2711del (p.Thr904LysfsTer?)
21g.18281042G>ACA318130072TMPRSS15c.2666C>T (p.Thr889Ile)
c.2801C>T (p.Thr934Ile)
c.2756C>T (p.Thr919Ile)
c.2720C>T (p.Thr907Ile)
c.2711C>T (p.Thr904Ile)
dbSNP gnomAD v4
21g.18281042G>CCA409847826TMPRSS15c.2666C>G (p.Thr889Arg)
c.2801C>G (p.Thr934Arg)
c.2756C>G (p.Thr919Arg)
c.2720C>G (p.Thr907Arg)
c.2711C>G (p.Thr904Arg)
21g.18281042G=CA2379736636TMPRSS15c.2666C= (p.Thr889=)
c.2801C= (p.Thr934=)
c.2756C= (p.Thr919=)
c.2720C= (p.Thr907=)
c.2711C= (p.Thr904=)
21g.18281042G>TCA409847827TMPRSS15c.2666C>A (p.Thr889Lys)
c.2801C>A (p.Thr934Lys)
c.2756C>A (p.Thr919Lys)
c.2720C>A (p.Thr907Lys)
c.2711C>A (p.Thr904Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.18281043T>ACA409847828TMPRSS15c.2665A>T (p.Thr889Ser)
c.2800A>T (p.Thr934Ser)
c.2755A>T (p.Thr919Ser)
c.2719A>T (p.Thr907Ser)
c.2710A>T (p.Thr904Ser)
21g.18281043T>CCA9983983TMPRSS15c.2665A>G (p.Thr889Ala)
c.2800A>G (p.Thr934Ala)
c.2755A>G (p.Thr919Ala)
c.2719A>G (p.Thr907Ala)
c.2710A>G (p.Thr904Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
21g.18281043T>GCA409847829TMPRSS15c.2665A>C (p.Thr889Pro)
c.2800A>C (p.Thr934Pro)
c.2755A>C (p.Thr919Pro)
c.2719A>C (p.Thr907Pro)
c.2710A>C (p.Thr904Pro)
21g.18281043T=CA2379736637TMPRSS15c.2665A= (p.Thr889=)
c.2800A= (p.Thr934=)
c.2755A= (p.Thr919=)
c.2719A= (p.Thr907=)
c.2710A= (p.Thr904=)
21g.18281044G>ACA511459089TMPRSS15c.2664C>T (p.Tyr888=)
c.2799C>T (p.Tyr933=)
c.2754C>T (p.Tyr918=)
c.2718C>T (p.Tyr906=)
c.2709C>T (p.Tyr903=)
dbSNP
21g.18281044G>CCA409847830TMPRSS15c.2664C>G (p.Tyr888Ter)
c.2799C>G (p.Tyr933Ter)
c.2754C>G (p.Tyr918Ter)
c.2718C>G (p.Tyr906Ter)
c.2709C>G (p.Tyr903Ter)
21g.18281044G=CA2379736638TMPRSS15c.2664C= (p.Tyr888=)
c.2799C= (p.Tyr933=)
c.2754C= (p.Tyr918=)
c.2718C= (p.Tyr906=)
c.2709C= (p.Tyr903=)
21g.18281044G>TCA409847831TMPRSS15c.2664C>A (p.Tyr888Ter)
c.2799C>A (p.Tyr933Ter)
c.2754C>A (p.Tyr918Ter)
c.2718C>A (p.Tyr906Ter)
c.2709C>A (p.Tyr903Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.18281045T>ACA409847832TMPRSS15c.2663A>T (p.Tyr888Phe)
c.2798A>T (p.Tyr933Phe)
c.2753A>T (p.Tyr918Phe)
c.2717A>T (p.Tyr906Phe)
c.2708A>T (p.Tyr903Phe)
21g.18281045T>CCA409847833TMPRSS15c.2663A>G (p.Tyr888Cys)
c.2798A>G (p.Tyr933Cys)
c.2753A>G (p.Tyr918Cys)
c.2717A>G (p.Tyr906Cys)
c.2708A>G (p.Tyr903Cys)
gnomAD v4
21g.18281045T>GCA409847834TMPRSS15c.2663A>C (p.Tyr888Ser)
c.2798A>C (p.Tyr933Ser)
c.2753A>C (p.Tyr918Ser)
c.2717A>C (p.Tyr906Ser)
c.2708A>C (p.Tyr903Ser)
21g.18281046A>CCA409847835TMPRSS15c.2662T>G (p.Tyr888Asp)
c.2797T>G (p.Tyr933Asp)
c.2752T>G (p.Tyr918Asp)
c.2716T>G (p.Tyr906Asp)
c.2707T>G (p.Tyr903Asp)
21g.18281046A>GCA409847836TMPRSS15c.2662T>C (p.Tyr888His)
c.2797T>C (p.Tyr933His)
c.2752T>C (p.Tyr918His)
c.2716T>C (p.Tyr906His)
c.2707T>C (p.Tyr903His)
21g.18281046A>TCA409847837TMPRSS15c.2662T>A (p.Tyr888Asn)
c.2797T>A (p.Tyr933Asn)
c.2752T>A (p.Tyr918Asn)
c.2716T>A (p.Tyr906Asn)
c.2707T>A (p.Tyr903Asn)
gnomAD v3 gnomAD v4
21g.18281047A>CCA409847838TMPRSS15c.2661T>G (p.Asn887Lys)
c.2796T>G (p.Asn932Lys)
c.2751T>G (p.Asn917Lys)
c.2715T>G (p.Asn905Lys)
c.2706T>G (p.Asn902Lys)
21g.18281047A>GCA511459090TMPRSS15c.2661T>C (p.Asn887=)
c.2796T>C (p.Asn932=)
c.2751T>C (p.Asn917=)
c.2715T>C (p.Asn905=)
c.2706T>C (p.Asn902=)
21g.18281047A>TCA409847839TMPRSS15c.2661T>A (p.Asn887Lys)
c.2796T>A (p.Asn932Lys)
c.2751T>A (p.Asn917Lys)
c.2715T>A (p.Asn905Lys)
c.2706T>A (p.Asn902Lys)
gnomAD v3 gnomAD v4
21g.18281048T>ACA409847841TMPRSS15c.2660A>T (p.Asn887Ile)
c.2795A>T (p.Asn932Ile)
c.2750A>T (p.Asn917Ile)
c.2714A>T (p.Asn905Ile)
c.2705A>T (p.Asn902Ile)
COSMIC
21g.18281048T>CCA409847842TMPRSS15c.2660A>G (p.Asn887Ser)
c.2795A>G (p.Asn932Ser)
c.2750A>G (p.Asn917Ser)
c.2714A>G (p.Asn905Ser)
c.2705A>G (p.Asn902Ser)
gnomAD v4
21g.18281048T>GCA409847840TMPRSS15c.2660A>C (p.Asn887Thr)
c.2795A>C (p.Asn932Thr)
c.2750A>C (p.Asn917Thr)
c.2714A>C (p.Asn905Thr)
c.2705A>C (p.Asn902Thr)
21g.18281049T>ACA409847843TMPRSS15c.2659A>T (p.Asn887Tyr)
c.2794A>T (p.Asn932Tyr)
c.2749A>T (p.Asn917Tyr)
c.2713A>T (p.Asn905Tyr)
c.2704A>T (p.Asn902Tyr)
21g.18281049T>CCA409847844TMPRSS15c.2659A>G (p.Asn887Asp)
c.2794A>G (p.Asn932Asp)
c.2749A>G (p.Asn917Asp)
c.2713A>G (p.Asn905Asp)
c.2704A>G (p.Asn902Asp)
21g.18281049T>GCA409847845TMPRSS15c.2659A>C (p.Asn887His)
c.2794A>C (p.Asn932His)
c.2749A>C (p.Asn917His)
c.2713A>C (p.Asn905His)
c.2704A>C (p.Asn902His)
21g.18281050C>ACA511459091TMPRSS15c.2658G>T (p.Val886=)
c.2793G>T (p.Val931=)
c.2748G>T (p.Val916=)
c.2712G>T (p.Val904=)
c.2703G>T (p.Val901=)
gnomAD v4
21g.18281050C=CA2379736639TMPRSS15c.2658G= (p.Val886=)
c.2793G= (p.Val931=)
c.2748G= (p.Val916=)
c.2712G= (p.Val904=)
c.2703G= (p.Val901=)
21g.18281050C>GCA511459092TMPRSS15c.2658G>C (p.Val886=)
c.2793G>C (p.Val931=)
c.2748G>C (p.Val916=)
c.2712G>C (p.Val904=)
c.2703G>C (p.Val901=)
21g.18281050C>TCA318130080TMPRSS15c.2658G>A (p.Val886=)
c.2793G>A (p.Val931=)
c.2748G>A (p.Val916=)
c.2712G>A (p.Val904=)
c.2703G>A (p.Val901=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.18281051A>CCA409847846TMPRSS15c.2657T>G (p.Val886Gly)
c.2792T>G (p.Val931Gly)
c.2747T>G (p.Val916Gly)
c.2711T>G (p.Val904Gly)
c.2702T>G (p.Val901Gly)
21g.18281051A>GCA409847847TMPRSS15c.2657T>C (p.Val886Ala)
c.2792T>C (p.Val931Ala)
c.2747T>C (p.Val916Ala)
c.2711T>C (p.Val904Ala)
c.2702T>C (p.Val901Ala)

Number of alleles fetched