Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.70853160A=CA2436261240TEX11c.406-7T= (n.406-7T=)
c.451-7T= (n.451-7T=)
Xg.70853160A>GCA877775999TEX11c.406-7T>C (n.406-7T>C)
c.451-7T>C (n.451-7T>C)
dbSNP gnomAD v4
Xg.70853161A=CA2436261241TEX11c.406-8T= (n.406-8T=)
c.451-8T= (n.451-8T=)
Xg.70853161A>TCA2436261242TEX11c.406-8T>A (n.406-8T>A)
c.451-8T>A (n.451-8T>A)
dbSNP
Xg.70853162T>CCA10442905TEX11c.406-9A>G (n.406-9A>G)
c.451-9A>G (n.451-9A>G)
dbSNP ExAC
Xg.70853162T=CA2436261243TEX11c.406-9A= (n.406-9A=)
c.451-9A= (n.451-9A=)
Xg.70853165A=CA2436261244TEX11c.406-12T= (n.406-12T=)
c.451-12T= (n.451-12T=)
Xg.70853165A>GCA642470359TEX11c.406-12T>C (n.406-12T>C)
c.451-12T>C (n.451-12T>C)
dbSNP gnomAD v2 gnomAD v4
Xg.70853168dupCA2694012961TEX11c.406-13dup (n.406-13dup)
c.451-13dup (n.451-13dup)
gnomAD v4
Xg.70853169A=CA2436261245TEX11c.406-16T= (n.406-16T=)
c.451-16T= (n.451-16T=)
Xg.70853169A>CCA2436261246TEX11c.406-16T>G (n.406-16T>G)
c.451-16T>G (n.451-16T>G)
dbSNP gnomAD v4
Xg.70853172G>ACA2579637143TEX11c.406-19C>T (n.406-19C>T)
c.451-19C>T (n.451-19C>T)
gnomAD v4
Xg.70853174A>GCA2694012962TEX11c.406-21T>C (n.406-21T>C)
c.451-21T>C (n.451-21T>C)
gnomAD v4
Xg.70853177_70853178delinsATCA2436261247TEX11c.406-25_406-24delinsAT (n.406-25_406-24delinsAT)
c.451-25_451-24delinsAT (n.451-25_451-24delinsAT)
Xg.70853178delCA642470360TEX11c.406-25del (n.406-25del)
c.451-25del (n.451-25del)
dbSNP gnomAD v2 gnomAD v4
Xg.70853178T>GCA2821714878TEX11c.406-25A>C (n.406-25A>C)
c.451-25A>C (n.451-25A>C)
Xg.70853183C>ACA642470361TEX11c.406-30G>T (n.406-30G>T)
c.451-30G>T (n.451-30G>T)
dbSNP gnomAD v2 gnomAD v4
Xg.70853183C=CA2436261248TEX11c.406-30G= (n.406-30G=)
c.451-30G= (n.451-30G=)
Xg.70853184A=CA2436261249TEX11c.406-31T= (n.406-31T=)
c.451-31T= (n.451-31T=)
Xg.70853184A>CCA331002040TEX11c.406-31T>G (n.406-31T>G)
c.451-31T>G (n.451-31T>G)
dbSNP gnomAD v2 gnomAD v4
Xg.70853184A>TCA2436261250TEX11c.406-31T>A (n.406-31T>A)
c.451-31T>A (n.451-31T>A)
dbSNP
Xg.70853185A>GCA2694012963TEX11c.406-32T>C (n.406-32T>C)
c.451-32T>C (n.451-32T>C)
gnomAD v4
Xg.70853186T>CCA2579637144TEX11c.406-33A>G (n.406-33A>G)
c.451-33A>G (n.451-33A>G)
Xg.70853189G>ACA642470362TEX11c.406-36C>T (n.406-36C>T)
c.451-36C>T (n.451-36C>T)
dbSNP gnomAD v2 gnomAD v4
Xg.70853189G=CA2436261251TEX11c.406-36C= (n.406-36C=)
c.451-36C= (n.451-36C=)
Xg.70853189_70853192delinsGAATCA2436261252TEX11c.406-39_406-36delinsATTC (n.406-39_406-36delinsATTC)
c.451-39_451-36delinsATTC (n.451-39_451-36delinsATTC)
Xg.70853192_70853194delCA877776028TEX11c.406-39_406-37del (n.406-39_406-37del)
c.451-39_451-37del (n.451-39_451-37del)
dbSNP
Xg.70853192T>CCA10442906TEX11c.406-39A>G (n.406-39A>G)
c.451-39A>G (n.451-39A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.70853192T=CA2436261253TEX11c.406-39A= (n.406-39A=)
c.451-39A= (n.451-39A=)
Xg.70853194A>TCA2694012964TEX11c.406-41T>A (n.406-41T>A)
c.451-41T>A (n.451-41T>A)
gnomAD v4
Xg.70853197A>CCA2694012965TEX11c.406-44T>G (n.406-44T>G)
c.451-44T>G (n.451-44T>G)
gnomAD v4
Xg.70853199A>GCA2694012966TEX11c.406-46T>C (n.406-46T>C)
c.451-46T>C (n.451-46T>C)
gnomAD v4
Xg.70853200G>CCA10442907TEX11c.406-47C>G (n.406-47C>G)
c.451-47C>G (n.451-47C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.70853200G=CA2436261254TEX11c.406-47C= (n.406-47C=)
c.451-47C= (n.451-47C=)
Xg.70853200G>TCA2694012967TEX11c.406-47C>A (n.406-47C>A)
c.451-47C>A (n.451-47C>A)
gnomAD v4
Xg.70853202T>CCA10442908TEX11c.405+46A>G (n.405+46A>G)
c.450+46A>G (n.450+46A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.70853202T=CA2436261255TEX11c.405+46A= (n.405+46A=)
c.450+46A= (n.450+46A=)
Xg.70853203G>ACA10442909TEX11c.405+45C>T (n.405+45C>T)
c.450+45C>T (n.450+45C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.70853203G=CA2436261256TEX11c.405+45C= (n.405+45C=)
c.450+45C= (n.450+45C=)
Xg.70853204T>CCA2694012968TEX11c.405+44A>G (n.405+44A>G)
c.450+44A>G (n.450+44A>G)
gnomAD v4
Xg.70853205T>GCA657714636TEX11c.405+43A>C (n.405+43A>C)
c.450+43A>C (n.450+43A>C)
COSMIC COSMIC
Xg.70853206A=CA2436261257TEX11c.405+42T= (n.405+42T=)
c.450+42T= (n.450+42T=)
Xg.70853206A>TCA10442910TEX11c.405+42T>A (n.405+42T>A)
c.450+42T>A (n.450+42T>A)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.70853213A=CA2436261258TEX11c.405+35T= (n.405+35T=)
c.450+35T= (n.450+35T=)
Xg.70853213A>CCA2436261259TEX11c.405+35T>G (n.405+35T>G)
c.450+35T>G (n.450+35T>G)
dbSNP gnomAD v4
Xg.70853214T>ACA1134089768TEX11c.405+34A>T (n.405+34A>T)
c.450+34A>T (n.450+34A>T)
dbSNP gnomAD v3 gnomAD v4
Xg.70853214T>CCA10442911TEX11c.405+34A>G (n.405+34A>G)
c.450+34A>G (n.450+34A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.70853214T=CA2436261260TEX11c.405+34A= (n.405+34A=)
c.450+34A= (n.450+34A=)
Xg.70853215A>GCA2694012969TEX11c.405+33T>C (n.405+33T>C)
c.450+33T>C (n.450+33T>C)
gnomAD v4
Xg.70853216A>GCA2694012970TEX11c.405+32T>C (n.405+32T>C)
c.450+32T>C (n.450+32T>C)
gnomAD v4
Xg.70853218T>CCA2579637145TEX11c.405+30A>G (n.405+30A>G)
c.450+30A>G (n.450+30A>G)
Xg.70853219G=CA2436261262TEX11c.405+29C= (n.405+29C=)
c.450+29C= (n.450+29C=)
Xg.70853219G>TCA2436261261TEX11c.405+29C>A (n.405+29C>A)
c.450+29C>A (n.450+29C>A)
dbSNP
Xg.70853220C>TCA2694012971TEX11c.405+28G>A (n.405+28G>A)
c.450+28G>A (n.450+28G>A)
gnomAD v4
Xg.70853221C>TCA2694012972TEX11c.405+27G>A (n.405+27G>A)
c.450+27G>A (n.450+27G>A)
gnomAD v4
Xg.70853223C=CA2436261263TEX11c.405+25G= (n.405+25G=)
c.450+25G= (n.450+25G=)
Xg.70853223C>TCA10442912TEX11c.405+25G>A (n.405+25G>A)
c.450+25G>A (n.450+25G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.70853224A=CA2436261264TEX11c.405+24T= (n.405+24T=)
c.450+24T= (n.450+24T=)
Xg.70853224A>GCA642470363TEX11c.405+24T>C (n.405+24T>C)
c.450+24T>C (n.450+24T>C)
dbSNP gnomAD v2 gnomAD v4
Xg.70853225G>ACA10442913TEX11c.405+23C>T (n.405+23C>T)
c.450+23C>T (n.450+23C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.70853225G=CA2436261265TEX11c.405+23C= (n.405+23C=)
c.450+23C= (n.450+23C=)
Xg.70853225G>TCA2579637146TEX11c.405+23C>A (n.405+23C>A)
c.450+23C>A (n.450+23C>A)
Xg.70853228A>GCA2694012973TEX11c.405+20T>C (n.405+20T>C)
c.450+20T>C (n.450+20T>C)
gnomAD v4
Xg.70853232G>CCA2694012975TEX11c.405+16C>G (n.405+16C>G)
c.450+16C>G (n.450+16C>G)
gnomAD v4
Xg.70853232G>TCA2694012974TEX11c.405+16C>A (n.405+16C>A)
c.450+16C>A (n.450+16C>A)
gnomAD v4
Xg.70853236A=CA2436261266TEX11c.405+12T= (n.405+12T=)
c.450+12T= (n.450+12T=)
Xg.70853236A>GCA2436261267TEX11c.405+12T>C (n.405+12T>C)
c.450+12T>C (n.450+12T>C)
dbSNP gnomAD v4
Xg.70853240T>CCA2558894188TEX11c.405+8A>G (n.405+8A>G)
c.450+8A>G (n.450+8A>G)
gnomAD v4
Xg.70853241A>GCA2694012976TEX11c.405+7T>C (n.405+7T>C)
c.450+7T>C (n.450+7T>C)
gnomAD v4
Xg.70853246A>CCA413608011TEX11c.405+2T>G (n.405+2T>G)
c.450+2T>G (n.450+2T>G)
Xg.70853246A>GCA413608012TEX11c.405+2T>C (n.405+2T>C)
c.450+2T>C (n.450+2T>C)
Xg.70853246A>TCA413608013TEX11c.405+2T>A (n.405+2T>A)
c.450+2T>A (n.450+2T>A)
Xg.70853247C>ACA413608014TEX11c.405+1G>T (n.405+1G>T)
c.450+1G>T (n.450+1G>T)
Xg.70853247C>GCA413608015TEX11c.405+1G>C (n.405+1G>C)
c.450+1G>C (n.450+1G>C)
Xg.70853247C>TCA413608016TEX11c.405+1G>A (n.405+1G>A)
c.450+1G>A (n.450+1G>A)
gnomAD v4
Xg.70853248G>ACA355011TEX11c.405C>T (p.Ala135=)
c.450C>T (p.Ala150=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.70853248G>CCA516759889TEX11c.405C>G (p.Ala135=)
c.450C>G (p.Ala150=)
Xg.70853248G=CA2436261268TEX11c.405C= (p.Ala135=)
c.450C= (p.Ala150=)
Xg.70853248G>TCA516759882TEX11c.405C>A (p.Ala135=)
c.450C>A (p.Ala150=)
COSMIC COSMIC
Xg.70853249G>ACA413608017TEX11c.404C>T (p.Ala135Val)
c.449C>T (p.Ala150Val)
Xg.70853249G>CCA413608018TEX11c.404C>G (p.Ala135Gly)
c.449C>G (p.Ala150Gly)
Xg.70853249G>TCA413608019TEX11c.404C>A (p.Ala135Asp)
c.449C>A (p.Ala150Asp)
Xg.70853250C>ACA413608020TEX11c.403G>T (p.Ala135Ser)
c.448G>T (p.Ala150Ser)
Xg.70853250C>GCA413608022TEX11c.403G>C (p.Ala135Pro)
c.448G>C (p.Ala150Pro)
Xg.70853250C>TCA413608021TEX11c.403G>A (p.Ala135Thr)
c.448G>A (p.Ala150Thr)
gnomAD v4
Xg.70853251C>ACA516759907TEX11c.402G>T (p.Val134=)
c.447G>T (p.Val149=)
Xg.70853251C>GCA516759906TEX11c.402G>C (p.Val134=)
c.447G>C (p.Val149=)
Xg.70853251C>TCA516759905TEX11c.402G>A (p.Val134=)
c.447G>A (p.Val149=)
Xg.70853252A>CCA413608023TEX11c.401T>G (p.Val134Gly)
c.446T>G (p.Val149Gly)
Xg.70853252A>GCA413608025TEX11c.401T>C (p.Val134Ala)
c.446T>C (p.Val149Ala)
Xg.70853252A>TCA413608024TEX11c.401T>A (p.Val134Glu)
c.446T>A (p.Val149Glu)
Xg.70853253C>ACA331002041TEX11c.400G>T (p.Val134Leu)
c.445G>T (p.Val149Leu)
dbSNP gnomAD v3 gnomAD v4
Xg.70853253C=CA2436261269TEX11c.400G= (p.Val134=)
c.445G= (p.Val149=)
Xg.70853253C>GCA413608026TEX11c.400G>C (p.Val134Leu)
c.445G>C (p.Val149Leu)
gnomAD v4
Xg.70853253C>TCA413608027TEX11c.400G>A (p.Val134Met)
c.445G>A (p.Val149Met)
Xg.70853254A=CA2436261270TEX11c.399T= (p.Ala133=)
c.444T= (p.Ala148=)
Xg.70853254A>CCA516759920TEX11c.399T>G (p.Ala133=)
c.444T>G (p.Ala148=)
Xg.70853254A>GCA10442914TEX11c.399T>C (p.Ala133=)
c.444T>C (p.Ala148=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.70853254A>TCA516759922TEX11c.399T>A (p.Ala133=)
c.444T>A (p.Ala148=)
Xg.70853255G>ACA413608028TEX11c.398C>T (p.Ala133Val)
c.443C>T (p.Ala148Val)
Xg.70853255G>CCA413608029TEX11c.398C>G (p.Ala133Gly)
c.443C>G (p.Ala148Gly)
Xg.70853255G>TCA413608030TEX11c.398C>A (p.Ala133Asp)
c.443C>A (p.Ala148Asp)
Xg.70853256C>ACA413608031TEX11c.397G>T (p.Ala133Ser)
c.442G>T (p.Ala148Ser)
Xg.70853256C>GCA413608032TEX11c.397G>C (p.Ala133Pro)
c.442G>C (p.Ala148Pro)
Xg.70853256C>TCA413608033TEX11c.397G>A (p.Ala133Thr)
c.442G>A (p.Ala148Thr)
Xg.70853257A=CA2436261271TEX11c.396T= (p.Ala132=)
c.441T= (p.Ala147=)
Xg.70853257A>CCA516759946TEX11c.396T>G (p.Ala132=)
c.441T>G (p.Ala147=)
Xg.70853257A>GCA516759949TEX11c.396T>C (p.Ala132=)
c.441T>C (p.Ala147=)
dbSNP gnomAD v4 COSMIC COSMIC
Xg.70853257A>TCA516759953TEX11c.396T>A (p.Ala132=)
c.441T>A (p.Ala147=)
Xg.70853258G>ACA413608034TEX11c.395C>T (p.Ala132Val)
c.440C>T (p.Ala147Val)
Xg.70853258G>CCA413608035TEX11c.395C>G (p.Ala132Gly)
c.440C>G (p.Ala147Gly)
Xg.70853258G>TCA413608036TEX11c.395C>A (p.Ala132Asp)
c.440C>A (p.Ala147Asp)

Number of alleles fetched