Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.37020625T>ACA359487284NIPBLc.5177T>A (p.Phe1726Tyr)
c.1-43953T>A (n.1-43953T>A)
c.4433T>A (p.Phe1478Tyr)
c.4979T>A (p.Phe1660Tyr)
c.4796T>A (p.Phe1599Tyr)
c.4517T>A (p.Phe1506Tyr)
c.3560T>A (p.Phe1187Tyr)
c.3551T>A (p.Phe1184Tyr)
5g.37020625T>CCA359487280NIPBLc.5177T>C (p.Phe1726Ser)
c.1-43953T>C (n.1-43953T>C)
c.4433T>C (p.Phe1478Ser)
c.4979T>C (p.Phe1660Ser)
c.4796T>C (p.Phe1599Ser)
c.4517T>C (p.Phe1506Ser)
c.3560T>C (p.Phe1187Ser)
c.3551T>C (p.Phe1184Ser)
5g.37020625T>GCA359487277NIPBLc.5177T>G (p.Phe1726Cys)
c.1-43953T>G (n.1-43953T>G)
c.4433T>G (p.Phe1478Cys)
c.4979T>G (p.Phe1660Cys)
c.4796T>G (p.Phe1599Cys)
c.4517T>G (p.Phe1506Cys)
c.3560T>G (p.Phe1187Cys)
c.3551T>G (p.Phe1184Cys)
5g.37020626T>ACA359487297NIPBLc.5178T>A (p.Phe1726Leu)
c.1-43952T>A (n.1-43952T>A)
c.4434T>A (p.Phe1478Leu)
c.4980T>A (p.Phe1660Leu)
c.4797T>A (p.Phe1599Leu)
c.4518T>A (p.Phe1506Leu)
c.3561T>A (p.Phe1187Leu)
c.3552T>A (p.Phe1184Leu)
gnomAD v4
5g.37020626T>CCA443905086NIPBLc.5178T>C (p.Phe1726=)
c.1-43952T>C (n.1-43952T>C)
c.4434T>C (p.Phe1478=)
c.4980T>C (p.Phe1660=)
c.4797T>C (p.Phe1599=)
c.4518T>C (p.Phe1506=)
c.3561T>C (p.Phe1187=)
c.3552T>C (p.Phe1184=)
5g.37020626T>GCA359487299NIPBLc.5178T>G (p.Phe1726Leu)
c.1-43952T>G (n.1-43952T>G)
c.4434T>G (p.Phe1478Leu)
c.4980T>G (p.Phe1660Leu)
c.4797T>G (p.Phe1599Leu)
c.4518T>G (p.Phe1506Leu)
c.3561T>G (p.Phe1187Leu)
c.3552T>G (p.Phe1184Leu)
5g.37020627C>ACA359487305NIPBLc.5179C>A (p.Leu1727Ile)
c.1-43951C>A (n.1-43951C>A)
c.4435C>A (p.Leu1479Ile)
c.4981C>A (p.Leu1661Ile)
c.4798C>A (p.Leu1600Ile)
c.4519C>A (p.Leu1507Ile)
c.3562C>A (p.Leu1188Ile)
c.3553C>A (p.Leu1185Ile)
5g.37020627C>GCA359487308NIPBLc.5179C>G (p.Leu1727Val)
c.1-43951C>G (n.1-43951C>G)
c.4435C>G (p.Leu1479Val)
c.4981C>G (p.Leu1661Val)
c.4798C>G (p.Leu1600Val)
c.4519C>G (p.Leu1507Val)
c.3562C>G (p.Leu1188Val)
c.3553C>G (p.Leu1185Val)
5g.37020627C>TCA359487311NIPBLc.5179C>T (p.Leu1727Phe)
c.1-43951C>T (n.1-43951C>T)
c.4435C>T (p.Leu1479Phe)
c.4981C>T (p.Leu1661Phe)
c.4798C>T (p.Leu1600Phe)
c.4519C>T (p.Leu1507Phe)
c.3562C>T (p.Leu1188Phe)
c.3553C>T (p.Leu1185Phe)
5g.37020628T>ACA359487314NIPBLc.5180T>A (p.Leu1727His)
c.1-43950T>A (n.1-43950T>A)
c.4436T>A (p.Leu1479His)
c.4982T>A (p.Leu1661His)
c.4799T>A (p.Leu1600His)
c.4520T>A (p.Leu1507His)
c.3563T>A (p.Leu1188His)
c.3554T>A (p.Leu1185His)
5g.37020628T>CCA359487324NIPBLc.5180T>C (p.Leu1727Pro)
c.1-43950T>C (n.1-43950T>C)
c.4436T>C (p.Leu1479Pro)
c.4982T>C (p.Leu1661Pro)
c.4799T>C (p.Leu1600Pro)
c.4520T>C (p.Leu1507Pro)
c.3563T>C (p.Leu1188Pro)
c.3554T>C (p.Leu1185Pro)
5g.37020628T>GCA359487326NIPBLc.5180T>G (p.Leu1727Arg)
c.1-43950T>G (n.1-43950T>G)
c.4436T>G (p.Leu1479Arg)
c.4982T>G (p.Leu1661Arg)
c.4799T>G (p.Leu1600Arg)
c.4520T>G (p.Leu1507Arg)
c.3563T>G (p.Leu1188Arg)
c.3554T>G (p.Leu1185Arg)
5g.37020629T>ACA443905088NIPBLc.5181T>A (p.Leu1727=)
c.1-43949T>A (n.1-43949T>A)
c.4437T>A (p.Leu1479=)
c.4983T>A (p.Leu1661=)
c.4800T>A (p.Leu1600=)
c.4521T>A (p.Leu1507=)
c.3564T>A (p.Leu1188=)
c.3555T>A (p.Leu1185=)
5g.37020629T>CCA443905089NIPBLc.5181T>C (p.Leu1727=)
c.1-43949T>C (n.1-43949T>C)
c.4437T>C (p.Leu1479=)
c.4983T>C (p.Leu1661=)
c.4800T>C (p.Leu1600=)
c.4521T>C (p.Leu1507=)
c.3564T>C (p.Leu1188=)
c.3555T>C (p.Leu1185=)
dbSNP gnomAD v4
5g.37020629T>GCA443905090NIPBLc.5181T>G (p.Leu1727=)
c.1-43949T>G (n.1-43949T>G)
c.4437T>G (p.Leu1479=)
c.4983T>G (p.Leu1661=)
c.4800T>G (p.Leu1600=)
c.4521T>G (p.Leu1507=)
c.3564T>G (p.Leu1188=)
c.3555T>G (p.Leu1185=)
5g.37020629T=CA1539583994NIPBLc.5181T= (p.Leu1727=)
c.1-43949T= (n.1-43949T=)
c.4437T= (p.Leu1479=)
c.4983T= (p.Leu1661=)
c.4800T= (p.Leu1600=)
c.4521T= (p.Leu1507=)
c.3564T= (p.Leu1188=)
c.3555T= (p.Leu1185=)
5g.37020630A=CA1539584001NIPBLc.5182A= (p.Arg1728=)
c.1-43948A= (n.1-43948A=)
c.4438A= (p.Arg1480=)
c.4984A= (p.Arg1662=)
c.4801A= (p.Arg1601=)
c.4522A= (p.Arg1508=)
c.3565A= (p.Arg1189=)
c.3556A= (p.Arg1186=)
5g.37020630A>CCA443905092NIPBLc.5182A>C (p.Arg1728=)
c.1-43948A>C (n.1-43948A>C)
c.4438A>C (p.Arg1480=)
c.4984A>C (p.Arg1662=)
c.4801A>C (p.Arg1601=)
c.4522A>C (p.Arg1508=)
c.3565A>C (p.Arg1189=)
c.3556A>C (p.Arg1186=)
5g.37020630A>GCA3236707NIPBLc.5182A>G (p.Arg1728Gly)
c.1-43948A>G (n.1-43948A>G)
c.4438A>G (p.Arg1480Gly)
c.4984A>G (p.Arg1662Gly)
c.4801A>G (p.Arg1601Gly)
c.4522A>G (p.Arg1508Gly)
c.3565A>G (p.Arg1189Gly)
c.3556A>G (p.Arg1186Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.37020630A>TCA359487334NIPBLc.5182A>T (p.Arg1728Ter)
c.1-43948A>T (n.1-43948A>T)
c.4438A>T (p.Arg1480Ter)
c.4984A>T (p.Arg1662Ter)
c.4801A>T (p.Arg1601Ter)
c.4522A>T (p.Arg1508Ter)
c.3565A>T (p.Arg1189Ter)
c.3556A>T (p.Arg1186Ter)
5g.37020631G>ACA359487338NIPBLc.5183G>A (p.Arg1728Lys)
c.1-43947G>A (n.1-43947G>A)
c.4439G>A (p.Arg1480Lys)
c.4985G>A (p.Arg1662Lys)
c.4802G>A (p.Arg1601Lys)
c.4523G>A (p.Arg1508Lys)
c.3566G>A (p.Arg1189Lys)
c.3557G>A (p.Arg1186Lys)
gnomAD v4
5g.37020631G>CCA359487343NIPBLc.5183G>C (p.Arg1728Thr)
c.1-43947G>C (n.1-43947G>C)
c.4439G>C (p.Arg1480Thr)
c.4985G>C (p.Arg1662Thr)
c.4802G>C (p.Arg1601Thr)
c.4523G>C (p.Arg1508Thr)
c.3566G>C (p.Arg1189Thr)
c.3557G>C (p.Arg1186Thr)
5g.37020631G>TCA359487341NIPBLc.5183G>T (p.Arg1728Ile)
c.1-43947G>T (n.1-43947G>T)
c.4439G>T (p.Arg1480Ile)
c.4985G>T (p.Arg1662Ile)
c.4802G>T (p.Arg1601Ile)
c.4523G>T (p.Arg1508Ile)
c.3566G>T (p.Arg1189Ile)
c.3557G>T (p.Arg1186Ile)
5g.37020632A=CA1539584006NIPBLc.5184A= (p.Arg1728=)
c.1-43946A= (n.1-43946A=)
c.4440A= (p.Arg1480=)
c.4986A= (p.Arg1662=)
c.4803A= (p.Arg1601=)
c.4524A= (p.Arg1508=)
c.3567A= (p.Arg1189=)
c.3558A= (p.Arg1186=)
5g.37020632A>CCA359487348NIPBLc.5184A>C (p.Arg1728Ser)
c.1-43946A>C (n.1-43946A>C)
c.4440A>C (p.Arg1480Ser)
c.4986A>C (p.Arg1662Ser)
c.4803A>C (p.Arg1601Ser)
c.4524A>C (p.Arg1508Ser)
c.3567A>C (p.Arg1189Ser)
c.3558A>C (p.Arg1186Ser)
5g.37020632A>GCA443905094NIPBLc.5184A>G (p.Arg1728=)
c.1-43946A>G (n.1-43946A>G)
c.4440A>G (p.Arg1480=)
c.4986A>G (p.Arg1662=)
c.4803A>G (p.Arg1601=)
c.4524A>G (p.Arg1508=)
c.3567A>G (p.Arg1189=)
c.3558A>G (p.Arg1186=)
5g.37020632A>TCA3236708NIPBLc.5184A>T (p.Arg1728Ser)
c.1-43946A>T (n.1-43946A>T)
c.4440A>T (p.Arg1480Ser)
c.4986A>T (p.Arg1662Ser)
c.4803A>T (p.Arg1601Ser)
c.4524A>T (p.Arg1508Ser)
c.3567A>T (p.Arg1189Ser)
c.3558A>T (p.Arg1186Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.37020633A>CCA359487353NIPBLc.5185A>C (p.Ser1729Arg)
c.1-43945A>C (n.1-43945A>C)
c.4441A>C (p.Ser1481Arg)
c.4987A>C (p.Ser1663Arg)
c.4804A>C (p.Ser1602Arg)
c.4525A>C (p.Ser1509Arg)
c.3568A>C (p.Ser1190Arg)
c.3559A>C (p.Ser1187Arg)
5g.37020633A>GCA359487355NIPBLc.5185A>G (p.Ser1729Gly)
c.1-43945A>G (n.1-43945A>G)
c.4441A>G (p.Ser1481Gly)
c.4987A>G (p.Ser1663Gly)
c.4804A>G (p.Ser1602Gly)
c.4525A>G (p.Ser1509Gly)
c.3568A>G (p.Ser1190Gly)
c.3559A>G (p.Ser1187Gly)
5g.37020633A>TCA359487360NIPBLc.5185A>T (p.Ser1729Cys)
c.1-43945A>T (n.1-43945A>T)
c.4441A>T (p.Ser1481Cys)
c.4987A>T (p.Ser1663Cys)
c.4804A>T (p.Ser1602Cys)
c.4525A>T (p.Ser1509Cys)
c.3568A>T (p.Ser1190Cys)
c.3559A>T (p.Ser1187Cys)
5g.37020634G>ACA359487363NIPBLc.5186G>A (p.Ser1729Asn)
c.1-43944G>A (n.1-43944G>A)
c.4442G>A (p.Ser1481Asn)
c.4988G>A (p.Ser1663Asn)
c.4805G>A (p.Ser1602Asn)
c.4526G>A (p.Ser1509Asn)
c.3569G>A (p.Ser1190Asn)
c.3560G>A (p.Ser1187Asn)
gnomAD v4
5g.37020634G>CCA359487366NIPBLc.5186G>C (p.Ser1729Thr)
c.1-43944G>C (n.1-43944G>C)
c.4442G>C (p.Ser1481Thr)
c.4988G>C (p.Ser1663Thr)
c.4805G>C (p.Ser1602Thr)
c.4526G>C (p.Ser1509Thr)
c.3569G>C (p.Ser1190Thr)
c.3560G>C (p.Ser1187Thr)
5g.37020634G>TCA359487364NIPBLc.5186G>T (p.Ser1729Ile)
c.1-43944G>T (n.1-43944G>T)
c.4442G>T (p.Ser1481Ile)
c.4988G>T (p.Ser1663Ile)
c.4805G>T (p.Ser1602Ile)
c.4526G>T (p.Ser1509Ile)
c.3569G>T (p.Ser1190Ile)
c.3560G>T (p.Ser1187Ile)
5g.37020635C>ACA359487369NIPBLc.5187C>A (p.Ser1729Arg)
c.1-43943C>A (n.1-43943C>A)
c.4443C>A (p.Ser1481Arg)
c.4989C>A (p.Ser1663Arg)
c.4806C>A (p.Ser1602Arg)
c.4527C>A (p.Ser1509Arg)
c.3570C>A (p.Ser1190Arg)
c.3561C>A (p.Ser1187Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.37020635C=CA1539584040NIPBLc.5187C= (p.Ser1729=)
c.1-43943C= (n.1-43943C=)
c.4443C= (p.Ser1481=)
c.4989C= (p.Ser1663=)
c.4806C= (p.Ser1602=)
c.4527C= (p.Ser1509=)
c.3570C= (p.Ser1190=)
c.3561C= (p.Ser1187=)
5g.37020635C>GCA359487371NIPBLc.5187C>G (p.Ser1729Arg)
c.1-43943C>G (n.1-43943C>G)
c.4443C>G (p.Ser1481Arg)
c.4989C>G (p.Ser1663Arg)
c.4806C>G (p.Ser1602Arg)
c.4527C>G (p.Ser1509Arg)
c.3570C>G (p.Ser1190Arg)
c.3561C>G (p.Ser1187Arg)
5g.37020635C>TCA117028018NIPBLc.5187C>T (p.Ser1729=)
c.1-43943C>T (n.1-43943C>T)
c.4443C>T (p.Ser1481=)
c.4989C>T (p.Ser1663=)
c.4806C>T (p.Ser1602=)
c.4527C>T (p.Ser1509=)
c.3570C>T (p.Ser1190=)
c.3561C>T (p.Ser1187=)
dbSNP gnomAD v2 gnomAD v4
5g.37020636A=CA1539584052NIPBLc.5188A= (p.Ile1730=)
c.1-43942A= (n.1-43942A=)
c.4444A= (p.Ile1482=)
c.4990A= (p.Ile1664=)
c.4807A= (p.Ile1603=)
c.4528A= (p.Ile1510=)
c.3571A= (p.Ile1191=)
c.3562A= (p.Ile1188=)
5g.37020636A>CCA359487374NIPBLc.5188A>C (p.Ile1730Leu)
c.1-43942A>C (n.1-43942A>C)
c.4444A>C (p.Ile1482Leu)
c.4990A>C (p.Ile1664Leu)
c.4807A>C (p.Ile1603Leu)
c.4528A>C (p.Ile1510Leu)
c.3571A>C (p.Ile1191Leu)
c.3562A>C (p.Ile1188Leu)
5g.37020636A>GCA3236709NIPBLc.5188A>G (p.Ile1730Val)
c.1-43942A>G (n.1-43942A>G)
c.4444A>G (p.Ile1482Val)
c.4990A>G (p.Ile1664Val)
c.4807A>G (p.Ile1603Val)
c.4528A>G (p.Ile1510Val)
c.3571A>G (p.Ile1191Val)
c.3562A>G (p.Ile1188Val)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.37020636A>TCA359487379NIPBLc.5188A>T (p.Ile1730Phe)
c.1-43942A>T (n.1-43942A>T)
c.4444A>T (p.Ile1482Phe)
c.4990A>T (p.Ile1664Phe)
c.4807A>T (p.Ile1603Phe)
c.4528A>T (p.Ile1510Phe)
c.3571A>T (p.Ile1191Phe)
c.3562A>T (p.Ile1188Phe)
5g.37020637T>ACA359487382NIPBLc.5189T>A (p.Ile1730Asn)
c.1-43941T>A (n.1-43941T>A)
c.4445T>A (p.Ile1482Asn)
c.4991T>A (p.Ile1664Asn)
c.4808T>A (p.Ile1603Asn)
c.4529T>A (p.Ile1510Asn)
c.3572T>A (p.Ile1191Asn)
c.3563T>A (p.Ile1188Asn)
5g.37020637T>CCA359487385NIPBLc.5189T>C (p.Ile1730Thr)
c.1-43941T>C (n.1-43941T>C)
c.4445T>C (p.Ile1482Thr)
c.4991T>C (p.Ile1664Thr)
c.4808T>C (p.Ile1603Thr)
c.4529T>C (p.Ile1510Thr)
c.3572T>C (p.Ile1191Thr)
c.3563T>C (p.Ile1188Thr)
5g.37020637T>GCA359487387NIPBLc.5189T>G (p.Ile1730Ser)
c.1-43941T>G (n.1-43941T>G)
c.4445T>G (p.Ile1482Ser)
c.4991T>G (p.Ile1664Ser)
c.4808T>G (p.Ile1603Ser)
c.4529T>G (p.Ile1510Ser)
c.3572T>G (p.Ile1191Ser)
c.3563T>G (p.Ile1188Ser)
5g.37020638T>ACA443905101NIPBLc.5190T>A (p.Ile1730=)
c.1-43940T>A (n.1-43940T>A)
c.4446T>A (p.Ile1482=)
c.4992T>A (p.Ile1664=)
c.4809T>A (p.Ile1603=)
c.4530T>A (p.Ile1510=)
c.3573T>A (p.Ile1191=)
c.3564T>A (p.Ile1188=)
5g.37020638T>CCA443905102NIPBLc.5190T>C (p.Ile1730=)
c.1-43940T>C (n.1-43940T>C)
c.4446T>C (p.Ile1482=)
c.4992T>C (p.Ile1664=)
c.4809T>C (p.Ile1603=)
c.4530T>C (p.Ile1510=)
c.3573T>C (p.Ile1191=)
c.3564T>C (p.Ile1188=)
5g.37020638T>GCA359487388NIPBLc.5190T>G (p.Ile1730Met)
c.1-43940T>G (n.1-43940T>G)
c.4446T>G (p.Ile1482Met)
c.4992T>G (p.Ile1664Met)
c.4809T>G (p.Ile1603Met)
c.4530T>G (p.Ile1510Met)
c.3573T>G (p.Ile1191Met)
c.3564T>G (p.Ile1188Met)
5g.37020639A=CA1539584056NIPBLc.5191A= (p.Ile1731=)
c.1-43939A= (n.1-43939A=)
c.4447A= (p.Ile1483=)
c.4993A= (p.Ile1665=)
c.4810A= (p.Ile1604=)
c.4531A= (p.Ile1511=)
c.3574A= (p.Ile1192=)
c.3565A= (p.Ile1189=)
5g.37020639A>CCA359487391NIPBLc.5191A>C (p.Ile1731Leu)
c.1-43939A>C (n.1-43939A>C)
c.4447A>C (p.Ile1483Leu)
c.4993A>C (p.Ile1665Leu)
c.4810A>C (p.Ile1604Leu)
c.4531A>C (p.Ile1511Leu)
c.3574A>C (p.Ile1192Leu)
c.3565A>C (p.Ile1189Leu)
5g.37020639A>GCA3236710NIPBLc.5191A>G (p.Ile1731Val)
c.1-43939A>G (n.1-43939A>G)
c.4447A>G (p.Ile1483Val)
c.4993A>G (p.Ile1665Val)
c.4810A>G (p.Ile1604Val)
c.4531A>G (p.Ile1511Val)
c.3574A>G (p.Ile1192Val)
c.3565A>G (p.Ile1189Val)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched