Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.36953700A>CCA359473442NIPBLc.4A>C (p.Asn2His)
c.-1+76678A>C (n.-1+76678A>C)
5g.36953700A>GCA359473443NIPBLc.4A>G (p.Asn2Asp)
c.-1+76678A>G (n.-1+76678A>G)
5g.36953700A>TCA359473444NIPBLc.4A>T (p.Asn2Tyr)
c.-1+76678A>T (n.-1+76678A>T)
5g.36953701A=CA1539571395NIPBLc.5A= (p.Asn2=)
c.-1+76679A= (n.-1+76679A=)
5g.36953701A>CCA359473445NIPBLc.5A>C (p.Asn2Thr)
c.-1+76679A>C (n.-1+76679A>C)
5g.36953701A>GCA359473447NIPBLc.5A>G (p.Asn2Ser)
c.-1+76679A>G (n.-1+76679A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.36953701A>TCA359473446NIPBLc.5A>T (p.Asn2Ile)
c.-1+76679A>T (n.-1+76679A>T)
5g.36953702T>ACA359473448NIPBLc.6T>A (p.Asn2Lys)
c.-1+76680T>A (n.-1+76680T>A)
5g.36953702T>CCA443901667NIPBLc.6T>C (p.Asn2=)
c.-1+76680T>C (n.-1+76680T>C)
5g.36953702T>GCA359473449NIPBLc.6T>G (p.Asn2Lys)
c.-1+76680T>G (n.-1+76680T>G)
5g.36953703G>ACA359473450NIPBLc.7G>A (p.Gly3Arg)
c.-1+76681G>A (n.-1+76681G>A)
gnomAD v4
5g.36953703G>CCA359473451NIPBLc.7G>C (p.Gly3Arg)
c.-1+76681G>C (n.-1+76681G>C)
5g.36953703G>TCA359473452NIPBLc.7G>T (p.Gly3Trp)
c.-1+76681G>T (n.-1+76681G>T)
5g.36953706dupCA2573052498NIPBLc.10dup (p.Asp4GlyfsTer15)
c.-1+76684dup (n.-1+76684dup)
ClinVar dbSNP
5g.36953704G>ACA359473453NIPBLc.8G>A (p.Gly3Glu)
c.-1+76682G>A (n.-1+76682G>A)
gnomAD v4
5g.36953704G>CCA359473454NIPBLc.8G>C (p.Gly3Ala)
c.-1+76682G>C (n.-1+76682G>C)
5g.36953704G>TCA359473455NIPBLc.8G>T (p.Gly3Val)
c.-1+76682G>T (n.-1+76682G>T)
5g.36953705G>ACA443901668NIPBLc.9G>A (p.Gly3=)
c.-1+76683G>A (n.-1+76683G>A)
gnomAD v4
5g.36953705G>CCA443901669NIPBLc.9G>C (p.Gly3=)
c.-1+76683G>C (n.-1+76683G>C)
5g.36953705G=CA1539571399NIPBLc.9G= (p.Gly3=)
c.-1+76683G= (n.-1+76683G=)
5g.36953705G>TCA443901670NIPBLc.9G>T (p.Gly3=)
c.-1+76683G>T (n.-1+76683G>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.36953706G>ACA359473456NIPBLc.10G>A (p.Asp4Asn)
c.-1+76684G>A (n.-1+76684G>A)
gnomAD v4
5g.36953706G>CCA359473457NIPBLc.10G>C (p.Asp4His)
c.-1+76684G>C (n.-1+76684G>C)
gnomAD v4
5g.36953706G>TCA359473458NIPBLc.10G>T (p.Asp4Tyr)
c.-1+76684G>T (n.-1+76684G>T)
5g.36953707A=CA1539571404NIPBLc.11A= (p.Asp4=)
c.-1+76685A= (n.-1+76685A=)
5g.36953707A>CCA359473459NIPBLc.11A>C (p.Asp4Ala)
c.-1+76685A>C (n.-1+76685A>C)
5g.36953707A>GCA359473460NIPBLc.11A>G (p.Asp4Gly)
c.-1+76685A>G (n.-1+76685A>G)
5g.36953707A>TCA117020953NIPBLc.11A>T (p.Asp4Val)
c.-1+76685A>T (n.-1+76685A>T)
dbSNP
5g.36953709_36953710dupCA2695204398NIPBLc.13_14dup (p.Met5IlefsTer20)
c.-1+76687_-1+76688dup (n.-1+76687_-1+76688dup)
5g.36953708T>ACA359473461NIPBLc.12T>A (p.Asp4Glu)
c.-1+76686T>A (n.-1+76686T>A)
5g.36953708T>CCA443901671NIPBLc.12T>C (p.Asp4=)
c.-1+76686T>C (n.-1+76686T>C)
5g.36953708T>GCA359473462NIPBLc.12T>G (p.Asp4Glu)
c.-1+76686T>G (n.-1+76686T>G)
5g.36953709A=CA1539571410NIPBLc.13A= (p.Met5=)
c.-1+76687A= (n.-1+76687A=)
5g.36953709A>CCA359473463NIPBLc.13A>C (p.Met5Leu)
c.-1+76687A>C (n.-1+76687A>C)
5g.36953709A>GCA359473464NIPBLc.13A>G (p.Met5Val)
c.-1+76687A>G (n.-1+76687A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.36953709A>TCA359473465NIPBLc.13A>T (p.Met5Leu)
c.-1+76687A>T (n.-1+76687A>T)
5g.36953710T>ACA359473466NIPBLc.14T>A (p.Met5Lys)
c.-1+76688T>A (n.-1+76688T>A)
5g.36953710T>CCA117020958NIPBLc.14T>C (p.Met5Thr)
c.-1+76688T>C (n.-1+76688T>C)
dbSNP
5g.36953710T>GCA3235726NIPBLc.14T>G (p.Met5Arg)
c.-1+76688T>G (n.-1+76688T>G)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.36953710T=CA1539571417NIPBLc.14T= (p.Met5=)
c.-1+76688T= (n.-1+76688T=)
5g.36953711G>ACA359473467NIPBLc.15G>A (p.Met5Ile)
c.-1+76689G>A (n.-1+76689G>A)
gnomAD v4
5g.36953711G>CCA359473468NIPBLc.15G>C (p.Met5Ile)
c.-1+76689G>C (n.-1+76689G>C)
5g.36953711G>TCA359473469NIPBLc.15G>T (p.Met5Ile)
c.-1+76689G>T (n.-1+76689G>T)
5g.36953712C>ACA359473470NIPBLc.16C>A (p.Pro6Thr)
c.-1+76690C>A (n.-1+76690C>A)
5g.36953712C>GCA359473471NIPBLc.16C>G (p.Pro6Ala)
c.-1+76690C>G (n.-1+76690C>G)
5g.36953712C>TCA359473472NIPBLc.16C>T (p.Pro6Ser)
c.-1+76690C>T (n.-1+76690C>T)
5g.36953715delCA2697547118NIPBLc.19del (p.His7MetfsTer17)
c.-1+76693del (n.-1+76693del)
ClinVar
5g.36953713C>ACA359473475NIPBLc.17C>A (p.Pro6His)
c.-1+76691C>A (n.-1+76691C>A)
5g.36953713C>GCA359473473NIPBLc.17C>G (p.Pro6Arg)
c.-1+76691C>G (n.-1+76691C>G)
5g.36953713C>TCA359473474NIPBLc.17C>T (p.Pro6Leu)
c.-1+76691C>T (n.-1+76691C>T)

Number of alleles fetched