Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.7582933_7587670delinsAGAACAGTCTTCA2580075482 ClinVar
6g.7582933_7587670delinsAGAGAAGAACAGTCTTCA915944145 ClinVar
6g.7582934_7587655delCA2695202641
6g.7583301_7585800delCA006686DSPc.4710_7209del (p.Gly1571GlufsTer?)
c.6039_8538del (p.Gly2014GlufsTer?)
c.4242_6741del (p.Gly1415GlufsTer?)
6g.7584407_7584423delCA2677219518DSPc.5816_5832del (p.Glu1939GlyfsTer2)
c.7145_7161del (p.Glu2382GlyfsTer2)
c.5348_5364del (p.Glu1783GlyfsTer2)
gnomAD v4
6g.7584415C>ACA362692354DSPc.5824C>A (p.Arg1942Ser)
c.7153C>A (p.Arg2385Ser)
c.5356C>A (p.Arg1786Ser)
gnomAD v4
6g.7584415C=CA1608611114DSPc.5824C= (p.Arg1942=)
c.7153C= (p.Arg2385=)
c.5356C= (p.Arg1786=)
6g.7584415C>GCA362692355DSPc.5824C>G (p.Arg1942Gly)
c.7153C>G (p.Arg2385Gly)
c.5356C>G (p.Arg1786Gly)
6g.7584415C>TCA049214DSPc.5824C>T (p.Arg1942Cys)
c.7153C>T (p.Arg2385Cys)
c.5356C>T (p.Arg1786Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7584416G>ACA362692356DSPc.5825G>A (p.Arg1942His)
c.7154G>A (p.Arg2385His)
c.5357G>A (p.Arg1786His)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.7584416G>CCA362692357DSPc.5825G>C (p.Arg1942Pro)
c.7154G>C (p.Arg2385Pro)
c.5357G>C (p.Arg1786Pro)
6g.7584416G=CA1608611122DSPc.5825G= (p.Arg1942=)
c.7154G= (p.Arg2385=)
c.5357G= (p.Arg1786=)
6g.7584416G>TCA362692358DSPc.5825G>T (p.Arg1942Leu)
c.7154G>T (p.Arg2385Leu)
c.5357G>T (p.Arg1786Leu)
6g.7584417T>ACA448716532DSPc.5826T>A (p.Arg1942=)
c.7155T>A (p.Arg2385=)
c.5358T>A (p.Arg1786=)
6g.7584417T>CCA448716534DSPc.5826T>C (p.Arg1942=)
c.7155T>C (p.Arg2385=)
c.5358T>C (p.Arg1786=)
6g.7584417T>GCA448716533DSPc.5826T>G (p.Arg1942=)
c.7155T>G (p.Arg2385=)
c.5358T>G (p.Arg1786=)
6g.7584418T>ACA362692359DSPc.5827T>A (p.Leu1943Ile)
c.7156T>A (p.Leu2386Ile)
c.5359T>A (p.Leu1787Ile)
6g.7584418T>CCA448716536DSPc.5827T>C (p.Leu1943=)
c.7156T>C (p.Leu2386=)
c.5359T>C (p.Leu1787=)
gnomAD v4
6g.7584418T>GCA362692360DSPc.5827T>G (p.Leu1943Val)
c.7156T>G (p.Leu2386Val)
c.5359T>G (p.Leu1787Val)
6g.7584419T>ACA362692361DSPc.5828T>A (p.Leu1943Ter)
c.7157T>A (p.Leu2386Ter)
c.5360T>A (p.Leu1787Ter)
6g.7584419T>CCA362692362DSPc.5828T>C (p.Leu1943Ser)
c.7157T>C (p.Leu2386Ser)
c.5360T>C (p.Leu1787Ser)
gnomAD v4
6g.7584419T>GCA362692363DSPc.5828T>G (p.Leu1943Ter)
c.7157T>G (p.Leu2386Ter)
c.5360T>G (p.Leu1787Ter)
6g.7584420A>CCA362692364DSPc.5829A>C (p.Leu1943Phe)
c.7158A>C (p.Leu2386Phe)
c.5361A>C (p.Leu1787Phe)
6g.7584420A>GCA448716543DSPc.5829A>G (p.Leu1943=)
c.7158A>G (p.Leu2386=)
c.5361A>G (p.Leu1787=)
6g.7584420A>TCA362692365DSPc.5829A>T (p.Leu1943Phe)
c.7158A>T (p.Leu2386Phe)
c.5361A>T (p.Leu1787Phe)
6g.7584421C>ACA362692366DSPc.5830C>A (p.Pro1944Thr)
c.7159C>A (p.Pro2387Thr)
c.5362C>A (p.Pro1788Thr)
6g.7584421C>GCA362692369DSPc.5830C>G (p.Pro1944Ala)
c.7159C>G (p.Pro2387Ala)
c.5362C>G (p.Pro1788Ala)
6g.7584421C>TCA362692367DSPc.5830C>T (p.Pro1944Ser)
c.7159C>T (p.Pro2387Ser)
c.5362C>T (p.Pro1788Ser)
6g.7584422C>ACA362692370DSPc.5831C>A (p.Pro1944Gln)
c.7160C>A (p.Pro2387Gln)
c.5363C>A (p.Pro1788Gln)
6g.7584422C=CA1608611132DSPc.5831C= (p.Pro1944=)
c.7160C= (p.Pro2387=)
c.5363C= (p.Pro1788=)
6g.7584422C>GCA362692371DSPc.5831C>G (p.Pro1944Arg)
c.7160C>G (p.Pro2387Arg)
c.5363C>G (p.Pro1788Arg)
6g.7584422C>TCA049230DSPc.5831C>T (p.Pro1944Leu)
c.7160C>T (p.Pro2387Leu)
c.5363C>T (p.Pro1788Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7584423A>CCA448716561DSPc.5832A>C (p.Pro1944=)
c.7161A>C (p.Pro2387=)
c.5364A>C (p.Pro1788=)
6g.7584423A>GCA448716562DSPc.5832A>G (p.Pro1944=)
c.7161A>G (p.Pro2387=)
c.5364A>G (p.Pro1788=)
6g.7584423A>TCA448716564DSPc.5832A>T (p.Pro1944=)
c.7161A>T (p.Pro2387=)
c.5364A>T (p.Pro1788=)
6g.7584424G>ACA049243DSPc.5833G>A (p.Val1945Ile)
c.7162G>A (p.Val2388Ile)
c.5365G>A (p.Val1789Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7584424G>CCA362692372DSPc.5833G>C (p.Val1945Leu)
c.7162G>C (p.Val2388Leu)
c.5365G>C (p.Val1789Leu)
6g.7584424G=CA1608611139DSPc.5833G= (p.Val1945=)
c.7162G= (p.Val2388=)
c.5365G= (p.Val1789=)
6g.7584424G>TCA362692373DSPc.5833G>T (p.Val1945Phe)
c.7162G>T (p.Val2388Phe)
c.5365G>T (p.Val1789Phe)
6g.7584425T>ACA362692374DSPc.5834T>A (p.Val1945Asp)
c.7163T>A (p.Val2388Asp)
c.5366T>A (p.Val1789Asp)
6g.7584425T>CCA362692375DSPc.5834T>C (p.Val1945Ala)
c.7163T>C (p.Val2388Ala)
c.5366T>C (p.Val1789Ala)
ClinVar
6g.7584425T>GCA362692376DSPc.5834T>G (p.Val1945Gly)
c.7163T>G (p.Val2388Gly)
c.5366T>G (p.Val1789Gly)
6g.7584426T>ACA448716575DSPc.5835T>A (p.Val1945=)
c.7164T>A (p.Val2388=)
c.5367T>A (p.Val1789=)
6g.7584426T>CCA448716576DSPc.5835T>C (p.Val1945=)
c.7164T>C (p.Val2388=)
c.5367T>C (p.Val1789=)
6g.7584426T>GCA448716578DSPc.5835T>G (p.Val1945=)
c.7164T>G (p.Val2388=)
c.5367T>G (p.Val1789=)
6g.7584427G>ACA362692377DSPc.5836G>A (p.Asp1946Asn)
c.7165G>A (p.Asp2389Asn)
c.5368G>A (p.Asp1790Asn)
6g.7584427G>CCA362692378DSPc.5836G>C (p.Asp1946His)
c.7165G>C (p.Asp2389His)
c.5368G>C (p.Asp1790His)
6g.7584427G>TCA362692379DSPc.5836G>T (p.Asp1946Tyr)
c.7165G>T (p.Asp2389Tyr)
c.5368G>T (p.Asp1790Tyr)
6g.7584428A>CCA362692380DSPc.5837A>C (p.Asp1946Ala)
c.7166A>C (p.Asp2389Ala)
c.5369A>C (p.Asp1790Ala)
6g.7584428A>GCA362692382DSPc.5837A>G (p.Asp1946Gly)
c.7166A>G (p.Asp2389Gly)
c.5369A>G (p.Asp1790Gly)

Number of alleles fetched