Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.7582933_7587670delinsAGAACAGTCTTCA2580075482 ClinVar
6g.7582933_7587670delinsAGAGAAGAACAGTCTTCA915944145 ClinVar
6g.7582934_7587655delCA2695202641
6g.7582987delCA351719DSPc.4396del (p.Ile1466LeufsTer20)
c.5725del (p.Ile1909LeufsTer20)
c.3928del (p.Ile1310LeufsTer20)
ClinVar dbSNP
6g.7582987A>CCA362689276DSPc.4396A>C (p.Ile1466Leu)
c.5725A>C (p.Ile1909Leu)
c.3928A>C (p.Ile1310Leu)
6g.7582987A>GCA362689277DSPc.4396A>G (p.Ile1466Val)
c.5725A>G (p.Ile1909Val)
c.3928A>G (p.Ile1310Val)
6g.7582987A>TCA362689278DSPc.4396A>T (p.Ile1466Phe)
c.5725A>T (p.Ile1909Phe)
c.3928A>T (p.Ile1310Phe)
6g.7582988T>ACA362689279DSPc.4397T>A (p.Ile1466Asn)
c.5726T>A (p.Ile1909Asn)
c.3929T>A (p.Ile1310Asn)
6g.7582988T>CCA045609DSPc.4397T>C (p.Ile1466Thr)
c.5726T>C (p.Ile1909Thr)
c.3929T>C (p.Ile1310Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7582988T>GCA362689280DSPc.4397T>G (p.Ile1466Ser)
c.5726T>G (p.Ile1909Ser)
c.3929T>G (p.Ile1310Ser)
6g.7582988T=CA1608606856DSPc.4397T= (p.Ile1466=)
c.5726T= (p.Ile1909=)
c.3929T= (p.Ile1310=)
6g.7582989T>ACA448715503DSPc.4398T>A (p.Ile1466=)
c.5727T>A (p.Ile1909=)
c.3930T>A (p.Ile1310=)
6g.7582989T>CCA448715504DSPc.4398T>C (p.Ile1466=)
c.5727T>C (p.Ile1909=)
c.3930T>C (p.Ile1310=)
gnomAD v4
6g.7582989T>GCA362689281DSPc.4398T>G (p.Ile1466Met)
c.5727T>G (p.Ile1909Met)
c.3930T>G (p.Ile1310Met)
6g.7582990G>ACA362689283DSPc.4399G>A (p.Glu1467Lys)
c.5728G>A (p.Glu1910Lys)
c.3931G>A (p.Glu1311Lys)
6g.7582990G>CCA362689284DSPc.4399G>C (p.Glu1467Gln)
c.5728G>C (p.Glu1910Gln)
c.3931G>C (p.Glu1311Gln)
6g.7582990G>TCA362689282DSPc.4399G>T (p.Glu1467Ter)
c.5728G>T (p.Glu1910Ter)
c.3931G>T (p.Glu1311Ter)
6g.7582991A>CCA362689285DSPc.4400A>C (p.Glu1467Ala)
c.5729A>C (p.Glu1910Ala)
c.3932A>C (p.Glu1311Ala)
6g.7582991A>GCA362689286DSPc.4400A>G (p.Glu1467Gly)
c.5729A>G (p.Glu1910Gly)
c.3932A>G (p.Glu1311Gly)
6g.7582991A>TCA362689287DSPc.4400A>T (p.Glu1467Val)
c.5729A>T (p.Glu1910Val)
c.3932A>T (p.Glu1311Val)
6g.7582992A>CCA362689288DSPc.4401A>C (p.Glu1467Asp)
c.5730A>C (p.Glu1910Asp)
c.3933A>C (p.Glu1311Asp)
6g.7582992A>GCA448715505DSPc.4401A>G (p.Glu1467=)
c.5730A>G (p.Glu1910=)
c.3933A>G (p.Glu1311=)
6g.7582992A>TCA362689289DSPc.4401A>T (p.Glu1467Asp)
c.5730A>T (p.Glu1910Asp)
c.3933A>T (p.Glu1311Asp)
6g.7582996_7582997dupCA2677234968DSPc.4405_4406dup (p.Cys1470GlyfsTer17)
c.5734_5735dup (p.Cys1913GlyfsTer17)
c.3937_3938dup (p.Cys1314GlyfsTer17)
gnomAD v4
6g.7582993G>ACA362689290DSPc.4402G>A (p.Glu1468Lys)
c.5731G>A (p.Glu1911Lys)
c.3934G>A (p.Glu1312Lys)
6g.7582993G>CCA362689291DSPc.4402G>C (p.Glu1468Gln)
c.5731G>C (p.Glu1911Gln)
c.3934G>C (p.Glu1312Gln)
6g.7582993G>TCA362689292DSPc.4402G>T (p.Glu1468Ter)
c.5731G>T (p.Glu1911Ter)
c.3934G>T (p.Glu1312Ter)
ClinVar
6g.7582994A>CCA362689293DSPc.4403A>C (p.Glu1468Ala)
c.5732A>C (p.Glu1911Ala)
c.3935A>C (p.Glu1312Ala)
6g.7582994A>GCA362689294DSPc.4403A>G (p.Glu1468Gly)
c.5732A>G (p.Glu1911Gly)
c.3935A>G (p.Glu1312Gly)
6g.7582994A>TCA362689295DSPc.4403A>T (p.Glu1468Val)
c.5732A>T (p.Glu1911Val)
c.3935A>T (p.Glu1312Val)
6g.7582995G>ACA448715506DSPc.4404G>A (p.Glu1468=)
c.5733G>A (p.Glu1911=)
c.3936G>A (p.Glu1312=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7582995G>CCA362689296DSPc.4404G>C (p.Glu1468Asp)
c.5733G>C (p.Glu1911Asp)
c.3936G>C (p.Glu1312Asp)
gnomAD v4
6g.7582995G=CA1608606859DSPc.4404G= (p.Glu1468=)
c.5733G= (p.Glu1911=)
c.3936G= (p.Glu1312=)
6g.7582995G>TCA362689297DSPc.4404G>T (p.Glu1468Asp)
c.5733G>T (p.Glu1911Asp)
c.3936G>T (p.Glu1312Asp)
6g.7582996A>CCA448715507DSPc.4405A>C (p.Arg1469=)
c.5734A>C (p.Arg1912=)
c.3937A>C (p.Arg1313=)
ClinVar
6g.7582996A>GCA362689299DSPc.4405A>G (p.Arg1469Gly)
c.5734A>G (p.Arg1912Gly)
c.3937A>G (p.Arg1313Gly)
6g.7582996A>TCA362689298DSPc.4405A>T (p.Arg1469Trp)
c.5734A>T (p.Arg1912Trp)
c.3937A>T (p.Arg1313Trp)
6g.7582997G>ACA362689300DSPc.4406G>A (p.Arg1469Lys)
c.5735G>A (p.Arg1912Lys)
c.3938G>A (p.Arg1313Lys)
6g.7582997G>CCA362689301DSPc.4406G>C (p.Arg1469Thr)
c.5735G>C (p.Arg1912Thr)
c.3938G>C (p.Arg1313Thr)
6g.7582997G>TCA362689302DSPc.4406G>T (p.Arg1469Met)
c.5735G>T (p.Arg1912Met)
c.3938G>T (p.Arg1313Met)
6g.7582998G>ACA045635DSPc.4407G>A (p.Arg1469=)
c.5736G>A (p.Arg1912=)
c.3939G>A (p.Arg1313=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7582998G>CCA362689303DSPc.4407G>C (p.Arg1469Ser)
c.5736G>C (p.Arg1912Ser)
c.3939G>C (p.Arg1313Ser)
6g.7582998G=CA1608606870DSPc.4407G= (p.Arg1469=)
c.5736G= (p.Arg1912=)
c.3939G= (p.Arg1313=)
6g.7582998G>TCA133972240DSPc.4407G>T (p.Arg1469Ser)
c.5736G>T (p.Arg1912Ser)
c.3939G>T (p.Arg1313Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7582999T>ACA362689304DSPc.4408T>A (p.Cys1470Ser)
c.5737T>A (p.Cys1913Ser)
c.3940T>A (p.Cys1314Ser)
6g.7582999T>CCA362689305DSPc.4408T>C (p.Cys1470Arg)
c.5737T>C (p.Cys1913Arg)
c.3940T>C (p.Cys1314Arg)
6g.7582999T>GCA362689306DSPc.4408T>G (p.Cys1470Gly)
c.5737T>G (p.Cys1913Gly)
c.3940T>G (p.Cys1314Gly)
6g.7583000G>ACA362689307DSPc.4409G>A (p.Cys1470Tyr)
c.5738G>A (p.Cys1913Tyr)
c.3941G>A (p.Cys1314Tyr)
6g.7583000G>CCA133972251DSPc.4409G>C (p.Cys1470Ser)
c.5738G>C (p.Cys1913Ser)
c.3941G>C (p.Cys1314Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583000G=CA1608606888DSPc.4409G= (p.Cys1470=)
c.5738G= (p.Cys1913=)
c.3941G= (p.Cys1314=)
6g.7583000G>TCA362689308DSPc.4409G>T (p.Cys1470Phe)
c.5738G>T (p.Cys1913Phe)
c.3941G>T (p.Cys1314Phe)
6g.7583001C>ACA362689309DSPc.4410C>A (p.Cys1470Ter)
c.5739C>A (p.Cys1913Ter)
c.3942C>A (p.Cys1314Ter)
6g.7583001C>GCA362689310DSPc.4410C>G (p.Cys1470Trp)
c.5739C>G (p.Cys1913Trp)
c.3942C>G (p.Cys1314Trp)
6g.7583001C>TCA448715508DSPc.4410C>T (p.Cys1470=)
c.5739C>T (p.Cys1913=)
c.3942C>T (p.Cys1314=)
6g.7583002A>CCA448715510DSPc.4411A>C (p.Arg1471=)
c.5740A>C (p.Arg1914=)
c.3943A>C (p.Arg1315=)
6g.7583002A>GCA362689311DSPc.4411A>G (p.Arg1471Gly)
c.5740A>G (p.Arg1914Gly)
c.3943A>G (p.Arg1315Gly)
gnomAD v4
6g.7583002A>TCA362689312DSPc.4411A>T (p.Arg1471Trp)
c.5740A>T (p.Arg1914Trp)
c.3943A>T (p.Arg1315Trp)
6g.7583002dupCA448715509DSPc.4411dup (p.Arg1471LysfsTer3)
c.5740dup (p.Arg1914LysfsTer3)
c.3943dup (p.Arg1315LysfsTer3)
6g.7583003G>ACA362689313DSPc.4412G>A (p.Arg1471Lys)
c.5741G>A (p.Arg1914Lys)
c.3944G>A (p.Arg1315Lys)
6g.7583003G>CCA362689315DSPc.4412G>C (p.Arg1471Thr)
c.5741G>C (p.Arg1914Thr)
c.3944G>C (p.Arg1315Thr)
6g.7583003G>TCA362689314DSPc.4412G>T (p.Arg1471Met)
c.5741G>T (p.Arg1914Met)
c.3944G>T (p.Arg1315Met)
6g.7583004G>ACA448715511DSPc.4413G>A (p.Arg1471=)
c.5742G>A (p.Arg1914=)
c.3945G>A (p.Arg1315=)
6g.7583004G>CCA362689316DSPc.4413G>C (p.Arg1471Ser)
c.5742G>C (p.Arg1914Ser)
c.3945G>C (p.Arg1315Ser)
6g.7583004G>TCA362689317DSPc.4413G>T (p.Arg1471Ser)
c.5742G>T (p.Arg1914Ser)
c.3945G>T (p.Arg1315Ser)
6g.7583005C>ACA362689318DSPc.4414C>A (p.Arg1472Ser)
c.5743C>A (p.Arg1915Ser)
c.3946C>A (p.Arg1316Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583005C=CA1608606900DSPc.4414C= (p.Arg1472=)
c.5743C= (p.Arg1915=)
c.3946C= (p.Arg1316=)
6g.7583005C>GCA362689319DSPc.4414C>G (p.Arg1472Gly)
c.5743C>G (p.Arg1915Gly)
c.3946C>G (p.Arg1316Gly)
6g.7583005C>TCA362689320DSPc.4414C>T (p.Arg1472Cys)
c.5743C>T (p.Arg1915Cys)
c.3946C>T (p.Arg1316Cys)
ClinVar dbSNP gnomAD v4
6g.7583006G>ACA006581DSPc.4415G>A (p.Arg1472His)
c.5744G>A (p.Arg1915His)
c.3947G>A (p.Arg1316His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583006G>CCA362689321DSPc.4415G>C (p.Arg1472Pro)
c.5744G>C (p.Arg1915Pro)
c.3947G>C (p.Arg1316Pro)
6g.7583006G=CA1608606909DSPc.4415G= (p.Arg1472=)
c.5744G= (p.Arg1915=)
c.3947G= (p.Arg1316=)
6g.7583006G>TCA362689322DSPc.4415G>T (p.Arg1472Leu)
c.5744G>T (p.Arg1915Leu)
c.3947G>T (p.Arg1316Leu)
6g.7583007T>ACA448715512DSPc.4416T>A (p.Arg1472=)
c.5745T>A (p.Arg1915=)
c.3948T>A (p.Arg1316=)
6g.7583007T>CCA448715513DSPc.4416T>C (p.Arg1472=)
c.5745T>C (p.Arg1915=)
c.3948T>C (p.Arg1316=)
ClinVar dbSNP
6g.7583007T>GCA448715514DSPc.4416T>G (p.Arg1472=)
c.5745T>G (p.Arg1915=)
c.3948T>G (p.Arg1316=)
6g.7583007dupCA16612041DSPc.4416dup (p.Lys1473Ter)
c.5745dup (p.Lys1916Ter)
c.3948dup (p.Lys1317Ter)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583008A>CCA362689323DSPc.4417A>C (p.Lys1473Gln)
c.5746A>C (p.Lys1916Gln)
c.3949A>C (p.Lys1317Gln)
6g.7583008A>GCA362689324DSPc.4417A>G (p.Lys1473Glu)
c.5746A>G (p.Lys1916Glu)
c.3949A>G (p.Lys1317Glu)
gnomAD v4
6g.7583008A>TCA362689325DSPc.4417A>T (p.Lys1473Ter)
c.5746A>T (p.Lys1916Ter)
c.3949A>T (p.Lys1317Ter)
6g.7583009A>CCA362689328DSPc.4418A>C (p.Lys1473Thr)
c.5747A>C (p.Lys1916Thr)
c.3950A>C (p.Lys1317Thr)
6g.7583009A>GCA362689327DSPc.4418A>G (p.Lys1473Arg)
c.5747A>G (p.Lys1916Arg)
c.3950A>G (p.Lys1317Arg)
6g.7583009A>TCA362689326DSPc.4418A>T (p.Lys1473Met)
c.5747A>T (p.Lys1916Met)
c.3950A>T (p.Lys1317Met)
6g.7583010G>ACA448715515DSPc.4419G>A (p.Lys1473=)
c.5748G>A (p.Lys1916=)
c.3951G>A (p.Lys1317=)
ClinVar
6g.7583010G>CCA362689329DSPc.4419G>C (p.Lys1473Asn)
c.5748G>C (p.Lys1916Asn)
c.3951G>C (p.Lys1317Asn)
6g.7583010G>TCA362689330DSPc.4419G>T (p.Lys1473Asn)
c.5748G>T (p.Lys1916Asn)
c.3951G>T (p.Lys1317Asn)
6g.7583011C>ACA362689331DSPc.4420C>A (p.Leu1474Met)
c.5749C>A (p.Leu1917Met)
c.3952C>A (p.Leu1318Met)
6g.7583011C=CA1608606916DSPc.4420C= (p.Leu1474=)
c.5749C= (p.Leu1917=)
c.3952C= (p.Leu1318=)
6g.7583011C>GCA133972258DSPc.4420C>G (p.Leu1474Val)
c.5749C>G (p.Leu1917Val)
c.3952C>G (p.Leu1318Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.7583011C>TCA448715516DSPc.4420C>T (p.Leu1474=)
c.5749C>T (p.Leu1917=)
c.3952C>T (p.Leu1318=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583012T>ACA362689332DSPc.4421T>A (p.Leu1474Gln)
c.5750T>A (p.Leu1917Gln)
c.3953T>A (p.Leu1318Gln)
6g.7583012T>CCA362689333DSPc.4421T>C (p.Leu1474Pro)
c.5750T>C (p.Leu1917Pro)
c.3953T>C (p.Leu1318Pro)
6g.7583012T>GCA362689334DSPc.4421T>G (p.Leu1474Arg)
c.5750T>G (p.Leu1917Arg)
c.3953T>G (p.Leu1318Arg)
6g.7583013G>ACA448715517DSPc.4422G>A (p.Leu1474=)
c.5751G>A (p.Leu1917=)
c.3954G>A (p.Leu1318=)
6g.7583013G>CCA448715518DSPc.4422G>C (p.Leu1474=)
c.5751G>C (p.Leu1917=)
c.3954G>C (p.Leu1318=)
6g.7583013G>TCA448715519DSPc.4422G>T (p.Leu1474=)
c.5751G>T (p.Leu1917=)
c.3954G>T (p.Leu1318=)
6g.7583014G>ACA362689335DSPc.4423G>A (p.Glu1475Lys)
c.5752G>A (p.Glu1918Lys)
c.3955G>A (p.Glu1319Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583014G>CCA362689336DSPc.4423G>C (p.Glu1475Gln)
c.5752G>C (p.Glu1918Gln)
c.3955G>C (p.Glu1319Gln)
6g.7583014G=CA1608606918DSPc.4423G= (p.Glu1475=)
c.5752G= (p.Glu1918=)
c.3955G= (p.Glu1319=)
6g.7583014G>TCA362689337DSPc.4423G>T (p.Glu1475Ter)
c.5752G>T (p.Glu1918Ter)
c.3955G>T (p.Glu1319Ter)
6g.7583015A=CA1608606919DSPc.4424A= (p.Glu1475=)
c.5753A= (p.Glu1918=)
c.3956A= (p.Glu1319=)
6g.7583015A>CCA362689338DSPc.4424A>C (p.Glu1475Ala)
c.5753A>C (p.Glu1918Ala)
c.3956A>C (p.Glu1319Ala)
dbSNP gnomAD v2 gnomAD v4
6g.7583015A>GCA362689339DSPc.4424A>G (p.Glu1475Gly)
c.5753A>G (p.Glu1918Gly)
c.3956A>G (p.Glu1319Gly)
6g.7583015A>TCA362689340DSPc.4424A>T (p.Glu1475Val)
c.5753A>T (p.Glu1918Val)
c.3956A>T (p.Glu1319Val)
6g.7583016G>ACA448715520DSPc.4425G>A (p.Glu1475=)
c.5754G>A (p.Glu1918=)
c.3957G>A (p.Glu1319=)
gnomAD v4
6g.7583016G>CCA362689341DSPc.4425G>C (p.Glu1475Asp)
c.5754G>C (p.Glu1918Asp)
c.3957G>C (p.Glu1319Asp)
6g.7583016G>TCA362689342DSPc.4425G>T (p.Glu1475Asp)
c.5754G>T (p.Glu1918Asp)
c.3957G>T (p.Glu1319Asp)
6g.7583017G>ACA362689343DSPc.4426G>A (p.Asp1476Asn)
c.5755G>A (p.Asp1919Asn)
c.3958G>A (p.Asp1320Asn)
6g.7583017G>CCA362689344DSPc.4426G>C (p.Asp1476His)
c.5755G>C (p.Asp1919His)
c.3958G>C (p.Asp1320His)
6g.7583017G=CA1608606921DSPc.4426G= (p.Asp1476=)
c.5755G= (p.Asp1919=)
c.3958G= (p.Asp1320=)
6g.7583017G>TCA362689345DSPc.4426G>T (p.Asp1476Tyr)
c.5755G>T (p.Asp1919Tyr)
c.3958G>T (p.Asp1320Tyr)
dbSNP gnomAD v2 gnomAD v4
6g.7583018A>CCA362689346DSPc.4427A>C (p.Asp1476Ala)
c.5756A>C (p.Asp1919Ala)
c.3959A>C (p.Asp1320Ala)
6g.7583018A>GCA362689347DSPc.4427A>G (p.Asp1476Gly)
c.5756A>G (p.Asp1919Gly)
c.3959A>G (p.Asp1320Gly)
6g.7583018A>TCA362689348DSPc.4427A>T (p.Asp1476Val)
c.5756A>T (p.Asp1919Val)
c.3959A>T (p.Asp1320Val)
gnomAD v4
6g.7583019T>ACA362689349DSPc.4428T>A (p.Asp1476Glu)
c.5757T>A (p.Asp1919Glu)
c.3960T>A (p.Asp1320Glu)
6g.7583019T>CCA448715521DSPc.4428T>C (p.Asp1476=)
c.5757T>C (p.Asp1919=)
c.3960T>C (p.Asp1320=)
6g.7583019T>GCA006588DSPc.4428T>G (p.Asp1476Glu)
c.5757T>G (p.Asp1919Glu)
c.3960T>G (p.Asp1320Glu)
ClinVar dbSNP gnomAD v4
6g.7583019T=CA1608606925DSPc.4428T= (p.Asp1476=)
c.5757T= (p.Asp1919=)
c.3960T= (p.Asp1320=)
6g.7583020T>ACA362689350DSPc.4429T>A (p.Ser1477Thr)
c.5758T>A (p.Ser1920Thr)
c.3961T>A (p.Ser1321Thr)
6g.7583020T>CCA362689351DSPc.4429T>C (p.Ser1477Pro)
c.5758T>C (p.Ser1920Pro)
c.3961T>C (p.Ser1321Pro)
6g.7583020T>GCA362689352DSPc.4429T>G (p.Ser1477Ala)
c.5758T>G (p.Ser1920Ala)
c.3961T>G (p.Ser1321Ala)
6g.7583021C>ACA362689353DSPc.4430C>A (p.Ser1477Tyr)
c.5759C>A (p.Ser1920Tyr)
c.3962C>A (p.Ser1321Tyr)
6g.7583021C>GCA362689354DSPc.4430C>G (p.Ser1477Cys)
c.5759C>G (p.Ser1920Cys)
c.3962C>G (p.Ser1321Cys)
6g.7583021C>TCA362689355DSPc.4430C>T (p.Ser1477Phe)
c.5759C>T (p.Ser1920Phe)
c.3962C>T (p.Ser1321Phe)
6g.7583022T>ACA448715522DSPc.4431T>A (p.Ser1477=)
c.5760T>A (p.Ser1920=)
c.3963T>A (p.Ser1321=)
6g.7583022T>CCA448715523DSPc.4431T>C (p.Ser1477=)
c.5760T>C (p.Ser1920=)
c.3963T>C (p.Ser1321=)
6g.7583022T>GCA448715524DSPc.4431T>G (p.Ser1477=)
c.5760T>G (p.Ser1920=)
c.3963T>G (p.Ser1321=)
6g.7583023A>CCA362689356DSPc.4432A>C (p.Thr1478Pro)
c.5761A>C (p.Thr1921Pro)
c.3964A>C (p.Thr1322Pro)
6g.7583023A>GCA362689358DSPc.4432A>G (p.Thr1478Ala)
c.5761A>G (p.Thr1921Ala)
c.3964A>G (p.Thr1322Ala)
6g.7583023A>TCA362689357DSPc.4432A>T (p.Thr1478Ser)
c.5761A>T (p.Thr1921Ser)
c.3964A>T (p.Thr1322Ser)
6g.7583025_7583033delCA2677234990DSPc.4434_4442del (p.Arg1479_Thr1481del)
c.5763_5771del (p.Arg1922_Thr1924del)
c.3966_3974del (p.Arg1323_Thr1325del)
gnomAD v4
6g.7583024C>ACA362689359DSPc.4433C>A (p.Thr1478Asn)
c.5762C>A (p.Thr1921Asn)
c.3965C>A (p.Thr1322Asn)
6g.7583024C>GCA362689360DSPc.4433C>G (p.Thr1478Ser)
c.5762C>G (p.Thr1921Ser)
c.3965C>G (p.Thr1322Ser)
6g.7583024C>TCA362689361DSPc.4433C>T (p.Thr1478Ile)
c.5762C>T (p.Thr1921Ile)
c.3965C>T (p.Thr1322Ile)
dbSNP gnomAD v3 gnomAD v4
6g.7583025C>ACA448715527DSPc.4434C>A (p.Thr1478=)
c.5763C>A (p.Thr1921=)
c.3966C>A (p.Thr1322=)
6g.7583025C=CA1608606931DSPc.4434C= (p.Thr1478=)
c.5763C= (p.Thr1921=)
c.3966C= (p.Thr1322=)
6g.7583025C>GCA448715525DSPc.4434C>G (p.Thr1478=)
c.5763C>G (p.Thr1921=)
c.3966C>G (p.Thr1322=)
6g.7583025C>TCA448715526DSPc.4434C>T (p.Thr1478=)
c.5763C>T (p.Thr1921=)
c.3966C>T (p.Thr1322=)
ClinVar dbSNP gnomAD v4
6g.7583025_7583026delinsCACA1608606929DSPc.4434_4435delinsCA (p.Thr1478=)
c.5763_5764delinsCA (p.Thr1921=)
c.3966_3967delinsCA (p.Thr1322=)
6g.7583026delCA045664DSPc.4435del (p.Arg1479GlyfsTer7)
c.5764del (p.Arg1922GlyfsTer7)
c.3967del (p.Arg1323GlyfsTer7)
dbSNP ExAC gnomAD v2
6g.7583026A>CCA448715528DSPc.4435A>C (p.Arg1479=)
c.5764A>C (p.Arg1922=)
c.3967A>C (p.Arg1323=)
6g.7583026A>GCA362689362DSPc.4435A>G (p.Arg1479Gly)
c.5764A>G (p.Arg1922Gly)
c.3967A>G (p.Arg1323Gly)
ClinVar
6g.7583026A>TCA362689363DSPc.4435A>T (p.Arg1479Trp)
c.5764A>T (p.Arg1922Trp)
c.3967A>T (p.Arg1323Trp)
6g.7583027G>ACA362689364DSPc.4436G>A (p.Arg1479Lys)
c.5765G>A (p.Arg1922Lys)
c.3968G>A (p.Arg1323Lys)
ClinVar dbSNP gnomAD v4
6g.7583027G>CCA362689365DSPc.4436G>C (p.Arg1479Thr)
c.5765G>C (p.Arg1922Thr)
c.3968G>C (p.Arg1323Thr)
6g.7583027G=CA1608606938DSPc.4436G= (p.Arg1479=)
c.5765G= (p.Arg1922=)
c.3968G= (p.Arg1323=)
6g.7583027G>TCA362689366DSPc.4436G>T (p.Arg1479Met)
c.5765G>T (p.Arg1922Met)
c.3968G>T (p.Arg1323Met)
6g.7583028G>ACA448715529DSPc.4437G>A (p.Arg1479=)
c.5766G>A (p.Arg1922=)
c.3969G>A (p.Arg1323=)
6g.7583028G>CCA362689367DSPc.4437G>C (p.Arg1479Ser)
c.5766G>C (p.Arg1922Ser)
c.3969G>C (p.Arg1323Ser)
dbSNP
6g.7583028G>TCA362689368DSPc.4437G>T (p.Arg1479Ser)
c.5766G>T (p.Arg1922Ser)
c.3969G>T (p.Arg1323Ser)
6g.7583029G>ACA006596DSPc.4438G>A (p.Glu1480Lys)
c.5767G>A (p.Glu1923Lys)
c.3970G>A (p.Glu1324Lys)
ClinVar dbSNP
6g.7583029G>CCA362689370DSPc.4438G>C (p.Glu1480Gln)
c.5767G>C (p.Glu1923Gln)
c.3970G>C (p.Glu1324Gln)
ClinVar dbSNP gnomAD v4
6g.7583029G=CA1608606948DSPc.4438G= (p.Glu1480=)
c.5767G= (p.Glu1923=)
c.3970G= (p.Glu1324=)
6g.7583029G>TCA362689369DSPc.4438G>T (p.Glu1480Ter)
c.5767G>T (p.Glu1923Ter)
c.3970G>T (p.Glu1324Ter)
6g.7583030A>CCA362689372DSPc.4439A>C (p.Glu1480Ala)
c.5768A>C (p.Glu1923Ala)
c.3971A>C (p.Glu1324Ala)
6g.7583030A>GCA362689371DSPc.4439A>G (p.Glu1480Gly)
c.5768A>G (p.Glu1923Gly)
c.3971A>G (p.Glu1324Gly)
6g.7583030A>TCA362689373DSPc.4439A>T (p.Glu1480Val)
c.5768A>T (p.Glu1923Val)
c.3971A>T (p.Glu1324Val)
6g.7583031G>ACA448715530DSPc.4440G>A (p.Glu1480=)
c.5769G>A (p.Glu1923=)
c.3972G>A (p.Glu1324=)
6g.7583031G>CCA362689374DSPc.4440G>C (p.Glu1480Asp)
c.5769G>C (p.Glu1923Asp)
c.3972G>C (p.Glu1324Asp)
6g.7583031G>TCA362689375DSPc.4440G>T (p.Glu1480Asp)
c.5769G>T (p.Glu1923Asp)
c.3972G>T (p.Glu1324Asp)
6g.7583031_7583033delinsGACCA1608606954DSPc.4440_4442delinsGAC (p.Glu1480=)
c.5769_5771delinsGAC (p.Glu1923=)
c.3972_3974delinsGAC (p.Glu1324=)
6g.7583032A>CCA362689376DSPc.4441A>C (p.Thr1481Pro)
c.5770A>C (p.Thr1924Pro)
c.3973A>C (p.Thr1325Pro)
6g.7583032A>GCA362689377DSPc.4441A>G (p.Thr1481Ala)
c.5770A>G (p.Thr1924Ala)
c.3973A>G (p.Thr1325Ala)
6g.7583032A>TCA362689378DSPc.4441A>T (p.Thr1481Ser)
c.5770A>T (p.Thr1924Ser)
c.3973A>T (p.Thr1325Ser)
6g.7583035_7583036delCA891843113DSPc.4444_4445del (p.Gln1482ValfsTer15)
c.5773_5774del (p.Gln1925ValfsTer15)
c.3976_3977del (p.Gln1326ValfsTer15)
ClinVar dbSNP
6g.7583033C>ACA362689379DSPc.4442C>A (p.Thr1481Lys)
c.5771C>A (p.Thr1924Lys)
c.3974C>A (p.Thr1325Lys)
6g.7583033C=CA1608606966DSPc.4442C= (p.Thr1481=)
c.5771C= (p.Thr1924=)
c.3974C= (p.Thr1325=)
6g.7583033C>GCA362689380DSPc.4442C>G (p.Thr1481Arg)
c.5771C>G (p.Thr1924Arg)
c.3974C>G (p.Thr1325Arg)
dbSNP gnomAD v2 gnomAD v4
6g.7583033C>TCA362689381DSPc.4442C>T (p.Thr1481Ile)
c.5771C>T (p.Thr1924Ile)
c.3974C>T (p.Thr1325Ile)
dbSNP
6g.7583034A>CCA448715531DSPc.4443A>C (p.Thr1481=)
c.5772A>C (p.Thr1924=)
c.3975A>C (p.Thr1325=)
6g.7583034A>GCA448715532DSPc.4443A>G (p.Thr1481=)
c.5772A>G (p.Thr1924=)
c.3975A>G (p.Thr1325=)
6g.7583034A>TCA448715533DSPc.4443A>T (p.Thr1481=)
c.5772A>T (p.Thr1924=)
c.3975A>T (p.Thr1325=)
6g.7583035C>ACA362689384DSPc.4444C>A (p.Gln1482Lys)
c.5773C>A (p.Gln1925Lys)
c.3976C>A (p.Gln1326Lys)
gnomAD v4
6g.7583035C>GCA362689382DSPc.4444C>G (p.Gln1482Glu)
c.5773C>G (p.Gln1925Glu)
c.3976C>G (p.Gln1326Glu)
6g.7583035C>TCA362689383DSPc.4444C>T (p.Gln1482Ter)
c.5773C>T (p.Gln1925Ter)
c.3976C>T (p.Gln1326Ter)
ClinVar dbSNP
6g.7583036A>CCA362689385DSPc.4445A>C (p.Gln1482Pro)
c.5774A>C (p.Gln1925Pro)
c.3977A>C (p.Gln1326Pro)
6g.7583036A>GCA362689386DSPc.4445A>G (p.Gln1482Arg)
c.5774A>G (p.Gln1925Arg)
c.3977A>G (p.Gln1326Arg)
COSMIC
6g.7583036A>TCA362689387DSPc.4445A>T (p.Gln1482Leu)
c.5774A>T (p.Gln1925Leu)
c.3977A>T (p.Gln1326Leu)
6g.7583037G>ACA448715534DSPc.4446G>A (p.Gln1482=)
c.5775G>A (p.Gln1925=)
c.3978G>A (p.Gln1326=)
dbSNP gnomAD v3 gnomAD v4
6g.7583037G>CCA362689388DSPc.4446G>C (p.Gln1482His)
c.5775G>C (p.Gln1925His)
c.3978G>C (p.Gln1326His)
6g.7583037G=CA1608606970DSPc.4446G= (p.Gln1482=)
c.5775G= (p.Gln1925=)
c.3978G= (p.Gln1326=)
6g.7583037G>TCA362689389DSPc.4446G>T (p.Gln1482His)
c.5775G>T (p.Gln1925His)
c.3978G>T (p.Gln1326His)
6g.7583038T>ACA362689390DSPc.4447T>A (p.Ser1483Thr)
c.5776T>A (p.Ser1926Thr)
c.3979T>A (p.Ser1327Thr)
gnomAD v4
6g.7583038T>CCA362689392DSPc.4447T>C (p.Ser1483Pro)
c.5776T>C (p.Ser1926Pro)
c.3979T>C (p.Ser1327Pro)
6g.7583038T>GCA362689391DSPc.4447T>G (p.Ser1483Ala)
c.5776T>G (p.Ser1926Ala)
c.3979T>G (p.Ser1327Ala)
6g.7583038_7583040delinsTCACA1608606982DSPc.4447_4449delinsTCA (p.Ser1483=)
c.5776_5778delinsTCA (p.Ser1926=)
c.3979_3981delinsTCA (p.Ser1327=)
6g.7583039C>ACA362689393DSPc.4448C>A (p.Ser1483Ter)
c.5777C>A (p.Ser1926Ter)
c.3980C>A (p.Ser1327Ter)
6g.7583039C>GCA362689394DSPc.4448C>G (p.Ser1483Ter)
c.5777C>G (p.Ser1926Ter)
c.3980C>G (p.Ser1327Ter)
6g.7583039C>TCA362689395DSPc.4448C>T (p.Ser1483Leu)
c.5777C>T (p.Ser1926Leu)
c.3980C>T (p.Ser1327Leu)
6g.7583041_7583042delCA1085707805DSPc.4450_4451del (p.Gln1484ValfsTer13)
c.5779_5780del (p.Gln1927ValfsTer13)
c.3982_3983del (p.Gln1328ValfsTer13)
dbSNP gnomAD v3 gnomAD v4
6g.7583040A>CCA448715535DSPc.4449A>C (p.Ser1483=)
c.5778A>C (p.Ser1926=)
c.3981A>C (p.Ser1327=)
6g.7583040A>GCA448715536DSPc.4449A>G (p.Ser1483=)
c.5778A>G (p.Ser1926=)
c.3981A>G (p.Ser1327=)
6g.7583040A>TCA448715537DSPc.4449A>T (p.Ser1483=)
c.5778A>T (p.Ser1926=)
c.3981A>T (p.Ser1327=)
6g.7583041C>ACA362689396DSPc.4450C>A (p.Gln1484Lys)
c.5779C>A (p.Gln1927Lys)
c.3982C>A (p.Gln1328Lys)
6g.7583041C=CA1608606997DSPc.4450C= (p.Gln1484=)
c.5779C= (p.Gln1927=)
c.3982C= (p.Gln1328=)
6g.7583041C>GCA006604DSPc.4450C>G (p.Gln1484Glu)
c.5779C>G (p.Gln1927Glu)
c.3982C>G (p.Gln1328Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583041C>TCA362689397DSPc.4450C>T (p.Gln1484Ter)
c.5779C>T (p.Gln1927Ter)
c.3982C>T (p.Gln1328Ter)
ClinVar gnomAD v4
6g.7583042A>CCA362689398DSPc.4451A>C (p.Gln1484Pro)
c.5780A>C (p.Gln1927Pro)
c.3983A>C (p.Gln1328Pro)
6g.7583042A>GCA362689399DSPc.4451A>G (p.Gln1484Arg)
c.5780A>G (p.Gln1927Arg)
c.3983A>G (p.Gln1328Arg)
6g.7583042A>TCA362689400DSPc.4451A>T (p.Gln1484Leu)
c.5780A>T (p.Gln1927Leu)
c.3983A>T (p.Gln1328Leu)
6g.7583044_7583047delCA2580075503DSPc.4453_4456del (p.Leu1485LysfsTer?)
c.5782_5785del (p.Leu1928LysfsTer?)
c.3985_3988del (p.Leu1329LysfsTer?)
ClinVar
6g.7583043G>ACA448715538DSPc.4452G>A (p.Gln1484=)
c.5781G>A (p.Gln1927=)
c.3984G>A (p.Gln1328=)
6g.7583043G>CCA362689401DSPc.4452G>C (p.Gln1484His)
c.5781G>C (p.Gln1927His)
c.3984G>C (p.Gln1328His)
6g.7583043G>TCA362689402DSPc.4452G>T (p.Gln1484His)
c.5781G>T (p.Gln1927His)
c.3984G>T (p.Gln1328His)
6g.7583044T>ACA362689404DSPc.4453T>A (p.Leu1485Ile)
c.5782T>A (p.Leu1928Ile)
c.3985T>A (p.Leu1329Ile)
6g.7583044T>CCA448715539DSPc.4453T>C (p.Leu1485=)
c.5782T>C (p.Leu1928=)
c.3985T>C (p.Leu1329=)
6g.7583044T>GCA362689403DSPc.4453T>G (p.Leu1485Val)
c.5782T>G (p.Leu1928Val)
c.3985T>G (p.Leu1329Val)
gnomAD v4
6g.7583045T>ACA362689405DSPc.4454T>A (p.Leu1485Ter)
c.5783T>A (p.Leu1928Ter)
c.3986T>A (p.Leu1329Ter)
6g.7583045T>CCA362689406DSPc.4454T>C (p.Leu1485Ser)
c.5783T>C (p.Leu1928Ser)
c.3986T>C (p.Leu1329Ser)
6g.7583045T>GCA362689407DSPc.4454T>G (p.Leu1485Ter)
c.5783T>G (p.Leu1928Ter)
c.3986T>G (p.Leu1329Ter)
6g.7583045_7583051delinsTAGAAACCA1608607004DSPc.4454_4460delinsTAGAAAC (p.Leu1485=)
c.5783_5789delinsTAGAAAC (p.Leu1928=)
c.3986_3992delinsTAGAAAC (p.Leu1329=)
6g.7583046A>CCA362689408DSPc.4455A>C (p.Leu1485Phe)
c.5784A>C (p.Leu1928Phe)
c.3987A>C (p.Leu1329Phe)
6g.7583046A>GCA448715540DSPc.4455A>G (p.Leu1485=)
c.5784A>G (p.Leu1928=)
c.3987A>G (p.Leu1329=)
6g.7583046A>TCA362689409DSPc.4455A>T (p.Leu1485Phe)
c.5784A>T (p.Leu1928Phe)
c.3987A>T (p.Leu1329Phe)
6g.7583050_7583055delCA565358152DSPc.4459_4464del (p.Thr1487_Glu1488del)
c.5788_5793del (p.Thr1930_Glu1931del)
c.3991_3996del (p.Thr1331_Glu1332del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583047G>ACA133972315DSPc.4456G>A (p.Glu1486Lys)
c.5785G>A (p.Glu1929Lys)
c.3988G>A (p.Glu1330Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583047G>CCA362689410DSPc.4456G>C (p.Glu1486Gln)
c.5785G>C (p.Glu1929Gln)
c.3988G>C (p.Glu1330Gln)
6g.7583047G=CA1608607012DSPc.4456G= (p.Glu1486=)
c.5785G= (p.Glu1929=)
c.3988G= (p.Glu1330=)
6g.7583047G>TCA362689411DSPc.4456G>T (p.Glu1486Ter)
c.5785G>T (p.Glu1929Ter)
c.3988G>T (p.Glu1330Ter)
6g.7583048A>CCA362689412DSPc.4457A>C (p.Glu1486Ala)
c.5786A>C (p.Glu1929Ala)
c.3989A>C (p.Glu1330Ala)
6g.7583048A>GCA362689413DSPc.4457A>G (p.Glu1486Gly)
c.5786A>G (p.Glu1929Gly)
c.3989A>G (p.Glu1330Gly)
6g.7583048A>TCA362689414DSPc.4457A>T (p.Glu1486Val)
c.5786A>T (p.Glu1929Val)
c.3989A>T (p.Glu1330Val)
6g.7583049A>CCA362689415DSPc.4458A>C (p.Glu1486Asp)
c.5787A>C (p.Glu1929Asp)
c.3990A>C (p.Glu1330Asp)
gnomAD v4
6g.7583049A>GCA448715541DSPc.4458A>G (p.Glu1486=)
c.5787A>G (p.Glu1929=)
c.3990A>G (p.Glu1330=)
6g.7583049A>TCA362689416DSPc.4458A>T (p.Glu1486Asp)
c.5787A>T (p.Glu1929Asp)
c.3990A>T (p.Glu1330Asp)
6g.7583050A>CCA362689419DSPc.4459A>C (p.Thr1487Pro)
c.5788A>C (p.Thr1930Pro)
c.3991A>C (p.Thr1331Pro)
6g.7583050A>GCA362689418DSPc.4459A>G (p.Thr1487Ala)
c.5788A>G (p.Thr1930Ala)
c.3991A>G (p.Thr1331Ala)
COSMIC
6g.7583050A>TCA362689417DSPc.4459A>T (p.Thr1487Ser)
c.5788A>T (p.Thr1930Ser)
c.3991A>T (p.Thr1331Ser)
6g.7583051C>ACA362689420DSPc.4460C>A (p.Thr1487Lys)
c.5789C>A (p.Thr1930Lys)
c.3992C>A (p.Thr1331Lys)
6g.7583051C=CA1608607020DSPc.4460C= (p.Thr1487=)
c.5789C= (p.Thr1930=)
c.3992C= (p.Thr1331=)
6g.7583051C>GCA006614DSPc.4460C>G (p.Thr1487Arg)
c.5789C>G (p.Thr1930Arg)
c.3992C>G (p.Thr1331Arg)
ClinVar dbSNP gnomAD v4
6g.7583051C>TCA362689421DSPc.4460C>T (p.Thr1487Ile)
c.5789C>T (p.Thr1930Ile)
c.3992C>T (p.Thr1331Ile)
6g.7583052A=CA1608607026DSPc.4461A= (p.Thr1487=)
c.5790A= (p.Thr1930=)
c.3993A= (p.Thr1331=)
6g.7583052A>CCA448715580DSPc.4461A>C (p.Thr1487=)
c.5790A>C (p.Thr1930=)
c.3993A>C (p.Thr1331=)
6g.7583052A>GCA448715581DSPc.4461A>G (p.Thr1487=)
c.5790A>G (p.Thr1930=)
c.3993A>G (p.Thr1331=)
ClinVar dbSNP gnomAD v4
6g.7583052A>TCA448715582DSPc.4461A>T (p.Thr1487=)
c.5790A>T (p.Thr1930=)
c.3993A>T (p.Thr1331=)
6g.7583053G>ACA362689422DSPc.4462G>A (p.Glu1488Lys)
c.5791G>A (p.Glu1931Lys)
c.3994G>A (p.Glu1332Lys)
6g.7583053G>CCA362689423DSPc.4462G>C (p.Glu1488Gln)
c.5791G>C (p.Glu1931Gln)
c.3994G>C (p.Glu1332Gln)
6g.7583053G>TCA362689424DSPc.4462G>T (p.Glu1488Ter)
c.5791G>T (p.Glu1931Ter)
c.3994G>T (p.Glu1332Ter)
6g.7583054A>CCA362689425DSPc.4463A>C (p.Glu1488Ala)
c.5792A>C (p.Glu1931Ala)
c.3995A>C (p.Glu1332Ala)
6g.7583054A>GCA362689426DSPc.4463A>G (p.Glu1488Gly)
c.5792A>G (p.Glu1931Gly)
c.3995A>G (p.Glu1332Gly)
6g.7583054A>TCA362689427DSPc.4463A>T (p.Glu1488Val)
c.5792A>T (p.Glu1931Val)
c.3995A>T (p.Glu1332Val)
6g.7583054_7583055insGAGTTAGATACA2677235036DSPc.4463_4464insGAGTTAGATA (p.Arg1489SerfsTer2)
c.5792_5793insGAGTTAGATA (p.Arg1932SerfsTer2)
c.3995_3996insGAGTTAGATA (p.Arg1333SerfsTer2)
gnomAD v4
6g.7583055A>CCA362689428DSPc.4464A>C (p.Glu1488Asp)
c.5793A>C (p.Glu1931Asp)
c.3996A>C (p.Glu1332Asp)
6g.7583055A>GCA448715585DSPc.4464A>G (p.Glu1488=)
c.5793A>G (p.Glu1931=)
c.3996A>G (p.Glu1332=)
6g.7583055A>TCA362689429DSPc.4464A>T (p.Glu1488Asp)
c.5793A>T (p.Glu1931Asp)
c.3996A>T (p.Glu1332Asp)
6g.7583056C>ACA362689430DSPc.4465C>A (p.Arg1489Ser)
c.5794C>A (p.Arg1932Ser)
c.3997C>A (p.Arg1333Ser)
6g.7583056C=CA1608607040DSPc.4465C= (p.Arg1489=)
c.5794C= (p.Arg1932=)
c.3997C= (p.Arg1333=)
6g.7583056C>GCA362689431DSPc.4465C>G (p.Arg1489Gly)
c.5794C>G (p.Arg1932Gly)
c.3997C>G (p.Arg1333Gly)
6g.7583056C>TCA045687DSPc.4465C>T (p.Arg1489Cys)
c.5794C>T (p.Arg1932Cys)
c.3997C>T (p.Arg1333Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.7583057G>ACA045698DSPc.4466G>A (p.Arg1489His)
c.5795G>A (p.Arg1932His)
c.3998G>A (p.Arg1333His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.7583057G>CCA362689433DSPc.4466G>C (p.Arg1489Pro)
c.5795G>C (p.Arg1932Pro)
c.3998G>C (p.Arg1333Pro)
6g.7583057G=CA1608607046DSPc.4466G= (p.Arg1489=)
c.5795G= (p.Arg1932=)
c.3998G= (p.Arg1333=)
6g.7583057G>TCA362689432DSPc.4466G>T (p.Arg1489Leu)
c.5795G>T (p.Arg1932Leu)
c.3998G>T (p.Arg1333Leu)
6g.7583058C>ACA448715587DSPc.4467C>A (p.Arg1489=)
c.5796C>A (p.Arg1932=)
c.3999C>A (p.Arg1333=)
6g.7583058C=CA1608607054DSPc.4467C= (p.Arg1489=)
c.5796C= (p.Arg1932=)
c.3999C= (p.Arg1333=)
6g.7583058C>GCA045714DSPc.4467C>G (p.Arg1489=)
c.5796C>G (p.Arg1932=)
c.3999C>G (p.Arg1333=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583058C>TCA045726DSPc.4467C>T (p.Arg1489=)
c.5796C>T (p.Arg1932=)
c.3999C>T (p.Arg1333=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583059T>ACA362689434DSPc.4468T>A (p.Ser1490Thr)
c.5797T>A (p.Ser1933Thr)
c.4000T>A (p.Ser1334Thr)
6g.7583059T>CCA362689435DSPc.4468T>C (p.Ser1490Pro)
c.5797T>C (p.Ser1933Pro)
c.4000T>C (p.Ser1334Pro)
6g.7583059T>GCA362689436DSPc.4468T>G (p.Ser1490Ala)
c.5797T>G (p.Ser1933Ala)
c.4000T>G (p.Ser1334Ala)
6g.7583060C>ACA362689437DSPc.4469C>A (p.Ser1490Tyr)
c.5798C>A (p.Ser1933Tyr)
c.4001C>A (p.Ser1334Tyr)
6g.7583060C=CA1608607062DSPc.4469C= (p.Ser1490=)
c.5798C= (p.Ser1933=)
c.4001C= (p.Ser1334=)
6g.7583060C>GCA362689438DSPc.4469C>G (p.Ser1490Cys)
c.5798C>G (p.Ser1933Cys)
c.4001C>G (p.Ser1334Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583060C>TCA133972347DSPc.4469C>T (p.Ser1490Phe)
c.5798C>T (p.Ser1933Phe)
c.4001C>T (p.Ser1334Phe)
ClinVar dbSNP
6g.7583061C>ACA448715589DSPc.4470C>A (p.Ser1490=)
c.5799C>A (p.Ser1933=)
c.4002C>A (p.Ser1334=)
6g.7583061C>GCA448715590DSPc.4470C>G (p.Ser1490=)
c.5799C>G (p.Ser1933=)
c.4002C>G (p.Ser1334=)
6g.7583061C>TCA448715591DSPc.4470C>T (p.Ser1490=)
c.5799C>T (p.Ser1933=)
c.4002C>T (p.Ser1334=)
6g.7583062C>ACA045761DSPc.4471C>A (p.Arg1491=)
c.5800C>A (p.Arg1934=)
c.4003C>A (p.Arg1335=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583062C=CA1608607078DSPc.4471C= (p.Arg1491=)
c.5800C= (p.Arg1934=)
c.4003C= (p.Arg1335=)
6g.7583062C>GCA362689439DSPc.4471C>G (p.Arg1491Gly)
c.5800C>G (p.Arg1934Gly)
c.4003C>G (p.Arg1335Gly)
gnomAD v4
6g.7583062C>TCA006621DSPc.4471C>T (p.Arg1491Ter)
c.5800C>T (p.Arg1934Ter)
c.4003C>T (p.Arg1335Ter)
ClinVar dbSNP
6g.7583063G>ACA362689440DSPc.4472G>A (p.Arg1491Gln)
c.5801G>A (p.Arg1934Gln)
c.4004G>A (p.Arg1335Gln)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.7583063G>CCA362689441DSPc.4472G>C (p.Arg1491Pro)
c.5801G>C (p.Arg1934Pro)
c.4004G>C (p.Arg1335Pro)
6g.7583063G=CA1608607087DSPc.4472G= (p.Arg1491=)
c.5801G= (p.Arg1934=)
c.4004G= (p.Arg1335=)
6g.7583063G>TCA362689442DSPc.4472G>T (p.Arg1491Leu)
c.5801G>T (p.Arg1934Leu)
c.4004G>T (p.Arg1335Leu)
ClinVar
6g.7583064A=CA1608607094DSPc.4473A= (p.Arg1491=)
c.5802A= (p.Arg1934=)
c.4005A= (p.Arg1335=)
6g.7583064A>CCA448715595DSPc.4473A>C (p.Arg1491=)
c.5802A>C (p.Arg1934=)
c.4005A>C (p.Arg1335=)
6g.7583064A>GCA448715596DSPc.4473A>G (p.Arg1491=)
c.5802A>G (p.Arg1934=)
c.4005A>G (p.Arg1335=)
ClinVar dbSNP
6g.7583064A>TCA448715597DSPc.4473A>T (p.Arg1491=)
c.5802A>T (p.Arg1934=)
c.4005A>T (p.Arg1335=)
ClinVar gnomAD v4
6g.7583065T>ACA362689445DSPc.4474T>A (p.Tyr1492Asn)
c.5803T>A (p.Tyr1935Asn)
c.4006T>A (p.Tyr1336Asn)
6g.7583065T>CCA362689443DSPc.4474T>C (p.Tyr1492His)
c.5803T>C (p.Tyr1935His)
c.4006T>C (p.Tyr1336His)
6g.7583065T>GCA362689444DSPc.4474T>G (p.Tyr1492Asp)
c.5803T>G (p.Tyr1935Asp)
c.4006T>G (p.Tyr1336Asp)
6g.7583066A=CA1608607101DSPc.4475A= (p.Tyr1492=)
c.5804A= (p.Tyr1935=)
c.4007A= (p.Tyr1336=)
6g.7583066A>CCA362689446DSPc.4475A>C (p.Tyr1492Ser)
c.5804A>C (p.Tyr1935Ser)
c.4007A>C (p.Tyr1336Ser)
6g.7583066A>GCA045770DSPc.4475A>G (p.Tyr1492Cys)
c.5804A>G (p.Tyr1935Cys)
c.4007A>G (p.Tyr1336Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583066A>TCA362689447DSPc.4475A>T (p.Tyr1492Phe)
c.5804A>T (p.Tyr1935Phe)
c.4007A>T (p.Tyr1336Phe)
6g.7583067T>ACA362689448DSPc.4476T>A (p.Tyr1492Ter)
c.5805T>A (p.Tyr1935Ter)
c.4008T>A (p.Tyr1336Ter)
6g.7583067T>CCA045784DSPc.4476T>C (p.Tyr1492=)
c.5805T>C (p.Tyr1935=)
c.4008T>C (p.Tyr1336=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583067T>GCA362689449DSPc.4476T>G (p.Tyr1492Ter)
c.5805T>G (p.Tyr1935Ter)
c.4008T>G (p.Tyr1336Ter)
6g.7583067T=CA1608607105DSPc.4476T= (p.Tyr1492=)
c.5805T= (p.Tyr1935=)
c.4008T= (p.Tyr1336=)
6g.7583068C>ACA362689450DSPc.4477C>A (p.Gln1493Lys)
c.5806C>A (p.Gln1936Lys)
c.4009C>A (p.Gln1337Lys)
6g.7583068C>GCA362689451DSPc.4477C>G (p.Gln1493Glu)
c.5806C>G (p.Gln1936Glu)
c.4009C>G (p.Gln1337Glu)
6g.7583068C>TCA362689452DSPc.4477C>T (p.Gln1493Ter)
c.5806C>T (p.Gln1936Ter)
c.4009C>T (p.Gln1337Ter)
ClinVar dbSNP
6g.7583069A=CA1608607111DSPc.4478A= (p.Gln1493=)
c.5807A= (p.Gln1936=)
c.4010A= (p.Gln1337=)
6g.7583069A>CCA362689453DSPc.4478A>C (p.Gln1493Pro)
c.5807A>C (p.Gln1936Pro)
c.4010A>C (p.Gln1337Pro)
6g.7583069A>GCA362689454DSPc.4478A>G (p.Gln1493Arg)
c.5807A>G (p.Gln1936Arg)
c.4010A>G (p.Gln1337Arg)
gnomAD v4
6g.7583069A>TCA362689455DSPc.4478A>T (p.Gln1493Leu)
c.5807A>T (p.Gln1936Leu)
c.4010A>T (p.Gln1337Leu)
ClinVar dbSNP gnomAD v4
6g.7583070G>ACA448715602DSPc.4479G>A (p.Gln1493=)
c.5808G>A (p.Gln1936=)
c.4011G>A (p.Gln1337=)
ClinVar
6g.7583070G>CCA045802DSPc.4479G>C (p.Gln1493His)
c.5808G>C (p.Gln1936His)
c.4011G>C (p.Gln1337His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
6g.7583070G=CA1608607118DSPc.4479G= (p.Gln1493=)
c.5808G= (p.Gln1936=)
c.4011G= (p.Gln1337=)
6g.7583070G>TCA362689456DSPc.4479G>T (p.Gln1493His)
c.5808G>T (p.Gln1936His)
c.4011G>T (p.Gln1337His)
6g.7583071A>CCA448715603DSPc.4480A>C (p.Arg1494=)
c.5809A>C (p.Arg1937=)
c.4012A>C (p.Arg1338=)
6g.7583071A>GCA362689457DSPc.4480A>G (p.Arg1494Gly)
c.5809A>G (p.Arg1937Gly)
c.4012A>G (p.Arg1338Gly)
6g.7583071A>TCA362689458DSPc.4480A>T (p.Arg1494Trp)
c.5809A>T (p.Arg1937Trp)
c.4012A>T (p.Arg1338Trp)
6g.7583072G>ACA045816DSPc.4481G>A (p.Arg1494Lys)
c.5810G>A (p.Arg1937Lys)
c.4013G>A (p.Arg1338Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583072G>CCA362689459DSPc.4481G>C (p.Arg1494Thr)
c.5810G>C (p.Arg1937Thr)
c.4013G>C (p.Arg1338Thr)
6g.7583072G=CA1608607120DSPc.4481G= (p.Arg1494=)
c.5810G= (p.Arg1937=)
c.4013G= (p.Arg1338=)
6g.7583072G>TCA362689460DSPc.4481G>T (p.Arg1494Met)
c.5810G>T (p.Arg1937Met)
c.4013G>T (p.Arg1338Met)
6g.7583073G>ACA448715605DSPc.4482G>A (p.Arg1494=)
c.5811G>A (p.Arg1937=)
c.4014G>A (p.Arg1338=)
6g.7583073G>CCA362689461DSPc.4482G>C (p.Arg1494Ser)
c.5811G>C (p.Arg1937Ser)
c.4014G>C (p.Arg1338Ser)
6g.7583073G>TCA362689462DSPc.4482G>T (p.Arg1494Ser)
c.5811G>T (p.Arg1937Ser)
c.4014G>T (p.Arg1338Ser)
6g.7583074G>ACA362689463DSPc.4483G>A (p.Glu1495Lys)
c.5812G>A (p.Glu1938Lys)
c.4015G>A (p.Glu1339Lys)
COSMIC
6g.7583074G>CCA362689464DSPc.4483G>C (p.Glu1495Gln)
c.5812G>C (p.Glu1938Gln)
c.4015G>C (p.Glu1339Gln)
ClinVar
6g.7583074G>TCA362689465DSPc.4483G>T (p.Glu1495Ter)
c.5812G>T (p.Glu1938Ter)
c.4015G>T (p.Glu1339Ter)
6g.7583075A>CCA362689466DSPc.4484A>C (p.Glu1495Ala)
c.5813A>C (p.Glu1938Ala)
c.4016A>C (p.Glu1339Ala)
6g.7583075A>GCA362689467DSPc.4484A>G (p.Glu1495Gly)
c.5813A>G (p.Glu1938Gly)
c.4016A>G (p.Glu1339Gly)
6g.7583075A>TCA362689468DSPc.4484A>T (p.Glu1495Val)
c.5813A>T (p.Glu1938Val)
c.4016A>T (p.Glu1339Val)
6g.7583076G>ACA448715609DSPc.4485G>A (p.Glu1495=)
c.5814G>A (p.Glu1938=)
c.4017G>A (p.Glu1339=)
gnomAD v4
6g.7583076G>CCA362689470DSPc.4485G>C (p.Glu1495Asp)
c.5814G>C (p.Glu1938Asp)
c.4017G>C (p.Glu1339Asp)
6g.7583076G>TCA362689469DSPc.4485G>T (p.Glu1495Asp)
c.5814G>T (p.Glu1938Asp)
c.4017G>T (p.Glu1339Asp)
6g.7583077A>CCA362689471DSPc.4486A>C (p.Ile1496Leu)
c.5815A>C (p.Ile1939Leu)
c.4018A>C (p.Ile1340Leu)
6g.7583077A>GCA362689472DSPc.4486A>G (p.Ile1496Val)
c.5815A>G (p.Ile1939Val)
c.4018A>G (p.Ile1340Val)
6g.7583077A>TCA362689473DSPc.4486A>T (p.Ile1496Phe)
c.5815A>T (p.Ile1939Phe)
c.4018A>T (p.Ile1340Phe)
6g.7583078T>ACA362689474DSPc.4487T>A (p.Ile1496Asn)
c.5816T>A (p.Ile1939Asn)
c.4019T>A (p.Ile1340Asn)
6g.7583078T>CCA362689475DSPc.4487T>C (p.Ile1496Thr)
c.5816T>C (p.Ile1939Thr)
c.4019T>C (p.Ile1340Thr)
ClinVar
6g.7583078T>GCA362689476DSPc.4487T>G (p.Ile1496Ser)
c.5816T>G (p.Ile1939Ser)
c.4019T>G (p.Ile1340Ser)
6g.7583079T>ACA448715613DSPc.4488T>A (p.Ile1496=)
c.5817T>A (p.Ile1939=)
c.4020T>A (p.Ile1340=)
6g.7583079T>CCA448715615DSPc.4488T>C (p.Ile1496=)
c.5817T>C (p.Ile1939=)
c.4020T>C (p.Ile1340=)
dbSNP gnomAD v2 gnomAD v4
6g.7583079T>GCA362689477DSPc.4488T>G (p.Ile1496Met)
c.5817T>G (p.Ile1939Met)
c.4020T>G (p.Ile1340Met)
gnomAD v4
6g.7583079T=CA1608607128DSPc.4488T= (p.Ile1496=)
c.5817T= (p.Ile1939=)
c.4020T= (p.Ile1340=)
6g.7583080G>ACA362689478DSPc.4489G>A (p.Asp1497Asn)
c.5818G>A (p.Asp1940Asn)
c.4021G>A (p.Asp1341Asn)
COSMIC
6g.7583080G>CCA362689479DSPc.4489G>C (p.Asp1497His)
c.5818G>C (p.Asp1940His)
c.4021G>C (p.Asp1341His)
6g.7583080G>TCA362689480DSPc.4489G>T (p.Asp1497Tyr)
c.5818G>T (p.Asp1940Tyr)
c.4021G>T (p.Asp1341Tyr)
6g.7583081A=CA1608607134DSPc.4490A= (p.Asp1497=)
c.5819A= (p.Asp1940=)
c.4022A= (p.Asp1341=)
6g.7583081A>CCA362689481DSPc.4490A>C (p.Asp1497Ala)
c.5819A>C (p.Asp1940Ala)
c.4022A>C (p.Asp1341Ala)
6g.7583081A>GCA362689482DSPc.4490A>G (p.Asp1497Gly)
c.5819A>G (p.Asp1940Gly)
c.4022A>G (p.Asp1341Gly)
6g.7583081A>TCA362689483DSPc.4490A>T (p.Asp1497Val)
c.5819A>T (p.Asp1940Val)
c.4022A>T (p.Asp1341Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7583082T>ACA362689485DSPc.4491T>A (p.Asp1497Glu)
c.5820T>A (p.Asp1940Glu)
c.4023T>A (p.Asp1341Glu)
6g.7583082T>CCA3628100DSPc.4491T>C (p.Asp1497=)
c.5820T>C (p.Asp1940=)
c.4023T>C (p.Asp1341=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
6g.7583082T>GCA362689484DSPc.4491T>G (p.Asp1497Glu)
c.5820T>G (p.Asp1940Glu)
c.4023T>G (p.Asp1341Glu)
6g.7583082T=CA1608607148DSPc.4491T= (p.Asp1497=)
c.5820T= (p.Asp1940=)
c.4023T= (p.Asp1341=)
6g.7583082_7583088delinsTAAACTCCA1608607153DSPc.4491_4497delinsTAAACTC (p.Asp1497=)
c.5820_5826delinsTAAACTC (p.Asp1940=)
c.4023_4029delinsTAAACTC (p.Asp1341=)
6g.7583083A=CA1608607166DSPc.4492A= (p.Lys1498=)
c.5821A= (p.Lys1941=)
c.4024A= (p.Lys1342=)
6g.7583083A>CCA362689486DSPc.4492A>C (p.Lys1498Gln)
c.5821A>C (p.Lys1941Gln)
c.4024A>C (p.Lys1342Gln)
6g.7583083A>GCA006629DSPc.4492A>G (p.Lys1498Glu)
c.5821A>G (p.Lys1941Glu)
c.4024A>G (p.Lys1342Glu)
ClinVar dbSNP
6g.7583083A>TCA362689487DSPc.4492A>T (p.Lys1498Ter)
c.5821A>T (p.Lys1941Ter)
c.4024A>T (p.Lys1342Ter)
6g.7583084_7583089delCA3628099DSPc.4493_4498del (p.Lys1498_Leu1499del)
c.5822_5827del (p.Lys1941_Leu1942del)
c.4025_4030del (p.Lys1342_Leu1343del)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.7583084A=CA1608607173DSPc.4493A= (p.Lys1498=)
c.5822A= (p.Lys1941=)
c.4025A= (p.Lys1342=)
6g.7583084A>CCA045860DSPc.4493A>C (p.Lys1498Thr)
c.5822A>C (p.Lys1941Thr)
c.4025A>C (p.Lys1342Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7583084A>GCA362689488DSPc.4493A>G (p.Lys1498Arg)
c.5822A>G (p.Lys1941Arg)
c.4025A>G (p.Lys1342Arg)
6g.7583084A>TCA362689489DSPc.4493A>T (p.Lys1498Ile)
c.5822A>T (p.Lys1941Ile)
c.4025A>T (p.Lys1342Ile)
6g.7583085A=CA1608607179DSPc.4494A= (p.Lys1498=)
c.5823A= (p.Lys1941=)
c.4026A= (p.Lys1342=)
6g.7583085A>CCA362689490DSPc.4494A>C (p.Lys1498Asn)
c.5823A>C (p.Lys1941Asn)
c.4026A>C (p.Lys1342Asn)
6g.7583085A>GCA133972444DSPc.4494A>G (p.Lys1498=)
c.5823A>G (p.Lys1941=)
c.4026A>G (p.Lys1342=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.7583085A>TCA362689491DSPc.4494A>T (p.Lys1498Asn)
c.5823A>T (p.Lys1941Asn)
c.4026A>T (p.Lys1342Asn)
6g.7583086C>ACA362689492DSPc.4495C>A (p.Leu1499Ile)
c.5824C>A (p.Leu1942Ile)
c.4027C>A (p.Leu1343Ile)
6g.7583086C>GCA362689493DSPc.4495C>G (p.Leu1499Val)
c.5824C>G (p.Leu1942Val)
c.4027C>G (p.Leu1343Val)
6g.7583086C>TCA362689494DSPc.4495C>T (p.Leu1499Phe)
c.5824C>T (p.Leu1942Phe)
c.4027C>T (p.Leu1343Phe)
6g.7583087T>ACA362689495DSPc.4496T>A (p.Leu1499His)
c.5825T>A (p.Leu1942His)
c.4028T>A (p.Leu1343His)
6g.7583087T>CCA362689496DSPc.4496T>C (p.Leu1499Pro)
c.5825T>C (p.Leu1942Pro)
c.4028T>C (p.Leu1343Pro)
6g.7583087T>GCA362689497DSPc.4496T>G (p.Leu1499Arg)
c.5825T>G (p.Leu1942Arg)
c.4028T>G (p.Leu1343Arg)

Number of alleles fetched