Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.177260159T>ACA362303400NSD1c.4264T>A (p.Cys1422Ser)
n.4720T>A
c.4828T>A (p.Cys1610Ser)
n.4534T>A
n.5284T>A
c.5137T>A (p.Cys1713Ser)
c.4330T>A (p.Cys1444Ser)
c.631T>A (p.Cys211Ser)
c.4717T>A (p.Cys1573Ser)
c.4081T>A (p.Cys1361Ser)
c.871T>A (p.Cys291Ser)
5g.177260159T>CCA362303401NSD1c.4264T>C (p.Cys1422Arg)
n.4720T>C
c.4828T>C (p.Cys1610Arg)
n.4534T>C
n.5284T>C
c.5137T>C (p.Cys1713Arg)
c.4330T>C (p.Cys1444Arg)
c.631T>C (p.Cys211Arg)
c.4717T>C (p.Cys1573Arg)
c.4081T>C (p.Cys1361Arg)
c.871T>C (p.Cys291Arg)
5g.177260159T>GCA362303402NSD1c.4264T>G (p.Cys1422Gly)
n.4720T>G
c.4828T>G (p.Cys1610Gly)
n.4534T>G
n.5284T>G
c.5137T>G (p.Cys1713Gly)
c.4330T>G (p.Cys1444Gly)
c.631T>G (p.Cys211Gly)
c.4717T>G (p.Cys1573Gly)
c.4081T>G (p.Cys1361Gly)
c.871T>G (p.Cys291Gly)
5g.177260160G>ACA362303403NSD1c.4265G>A (p.Cys1422Tyr)
n.4721G>A
c.4829G>A (p.Cys1610Tyr)
n.4535G>A
n.5285G>A
c.5138G>A (p.Cys1713Tyr)
c.4331G>A (p.Cys1444Tyr)
c.632G>A (p.Cys211Tyr)
c.4718G>A (p.Cys1573Tyr)
c.4082G>A (p.Cys1361Tyr)
c.872G>A (p.Cys291Tyr)
dbSNP
5g.177260160G>CCA362303404NSD1c.4265G>C (p.Cys1422Ser)
n.4721G>C
c.4829G>C (p.Cys1610Ser)
n.4535G>C
n.5285G>C
c.5138G>C (p.Cys1713Ser)
c.4331G>C (p.Cys1444Ser)
c.632G>C (p.Cys211Ser)
c.4718G>C (p.Cys1573Ser)
c.4082G>C (p.Cys1361Ser)
c.872G>C (p.Cys291Ser)
5g.177260160G>TCA362303405NSD1c.4265G>T (p.Cys1422Phe)
n.4721G>T
c.4829G>T (p.Cys1610Phe)
n.4535G>T
n.5285G>T
c.5138G>T (p.Cys1713Phe)
c.4331G>T (p.Cys1444Phe)
c.632G>T (p.Cys211Phe)
c.4718G>T (p.Cys1573Phe)
c.4082G>T (p.Cys1361Phe)
c.872G>T (p.Cys291Phe)
5g.177260161C>ACA362303408NSD1c.4266C>A (p.Cys1422Ter)
n.4722C>A
c.4830C>A (p.Cys1610Ter)
n.4536C>A
n.5286C>A
c.5139C>A (p.Cys1713Ter)
c.4332C>A (p.Cys1444Ter)
c.633C>A (p.Cys211Ter)
c.4719C>A (p.Cys1573Ter)
c.4083C>A (p.Cys1361Ter)
c.873C>A (p.Cys291Ter)
5g.177260161C>GCA362303406NSD1c.4266C>G (p.Cys1422Trp)
n.4722C>G
c.4830C>G (p.Cys1610Trp)
n.4536C>G
n.5286C>G
c.5139C>G (p.Cys1713Trp)
c.4332C>G (p.Cys1444Trp)
c.633C>G (p.Cys211Trp)
c.4719C>G (p.Cys1573Trp)
c.4083C>G (p.Cys1361Trp)
c.873C>G (p.Cys291Trp)
5g.177260161C>TCA447726432NSD1c.4266C>T (p.Cys1422=)
n.4722C>T
c.4830C>T (p.Cys1610=)
n.4536C>T
n.5286C>T
c.5139C>T (p.Cys1713=)
c.4332C>T (p.Cys1444=)
c.633C>T (p.Cys211=)
c.4719C>T (p.Cys1573=)
c.4083C>T (p.Cys1361=)
c.873C>T (p.Cys291=)
COSMIC COSMIC
5g.177260162T>ACA362303411NSD1c.4267T>A (p.Ser1423Thr)
n.4723T>A
c.4831T>A (p.Ser1611Thr)
n.4537T>A
n.5287T>A
c.5140T>A (p.Ser1714Thr)
c.4333T>A (p.Ser1445Thr)
c.634T>A (p.Ser212Thr)
c.4720T>A (p.Ser1574Thr)
c.4084T>A (p.Ser1362Thr)
c.874T>A (p.Ser292Thr)
dbSNP
5g.177260162T>CCA362303413NSD1c.4267T>C (p.Ser1423Pro)
n.4723T>C
c.4831T>C (p.Ser1611Pro)
n.4537T>C
n.5287T>C
c.5140T>C (p.Ser1714Pro)
c.4333T>C (p.Ser1445Pro)
c.634T>C (p.Ser212Pro)
c.4720T>C (p.Ser1574Pro)
c.4084T>C (p.Ser1362Pro)
c.874T>C (p.Ser292Pro)
5g.177260162T>GCA362303415NSD1c.4267T>G (p.Ser1423Ala)
n.4723T>G
c.4831T>G (p.Ser1611Ala)
n.4537T>G
n.5287T>G
c.5140T>G (p.Ser1714Ala)
c.4333T>G (p.Ser1445Ala)
c.634T>G (p.Ser212Ala)
c.4720T>G (p.Ser1574Ala)
c.4084T>G (p.Ser1362Ala)
c.874T>G (p.Ser292Ala)
5g.177260163C>ACA362303417NSD1c.4268C>A (p.Ser1423Ter)
n.4724C>A
c.4832C>A (p.Ser1611Ter)
n.4538C>A
n.5288C>A
c.5141C>A (p.Ser1714Ter)
c.4334C>A (p.Ser1445Ter)
c.635C>A (p.Ser212Ter)
c.4721C>A (p.Ser1574Ter)
c.4085C>A (p.Ser1362Ter)
c.875C>A (p.Ser292Ter)
5g.177260163C=CA1603527299NSD1c.4268C= (p.Ser1423=)
n.4724C=
c.4832C= (p.Ser1611=)
n.4538C=
n.5288C=
c.5141C= (p.Ser1714=)
c.4334C= (p.Ser1445=)
c.635C= (p.Ser212=)
c.4721C= (p.Ser1574=)
c.4085C= (p.Ser1362=)
c.875C= (p.Ser292=)
5g.177260163C>GCA294936NSD1c.4268C>G (p.Ser1423Ter)
n.4724C>G
c.4832C>G (p.Ser1611Ter)
n.4538C>G
n.5288C>G
c.5141C>G (p.Ser1714Ter)
c.4334C>G (p.Ser1445Ter)
c.635C>G (p.Ser212Ter)
c.4721C>G (p.Ser1574Ter)
c.4085C>G (p.Ser1362Ter)
c.875C>G (p.Ser292Ter)
ClinVar dbSNP
5g.177260163C>TCA362303419NSD1c.4268C>T (p.Ser1423Leu)
n.4724C>T
c.4832C>T (p.Ser1611Leu)
n.4538C>T
n.5288C>T
c.5141C>T (p.Ser1714Leu)
c.4334C>T (p.Ser1445Leu)
c.635C>T (p.Ser212Leu)
c.4721C>T (p.Ser1574Leu)
c.4085C>T (p.Ser1362Leu)
c.875C>T (p.Ser292Leu)
5g.177260164A=CA1603527309NSD1c.4269A= (p.Ser1423=)
n.4725A=
c.4833A= (p.Ser1611=)
n.4539A=
n.5289A=
c.5142A= (p.Ser1714=)
c.4335A= (p.Ser1445=)
c.636A= (p.Ser212=)
c.4722A= (p.Ser1574=)
c.4086A= (p.Ser1362=)
c.876A= (p.Ser292=)
5g.177260164A>CCA447726433NSD1c.4269A>C (p.Ser1423=)
n.4725A>C
c.4833A>C (p.Ser1611=)
n.4539A>C
n.5289A>C
c.5142A>C (p.Ser1714=)
c.4335A>C (p.Ser1445=)
c.636A>C (p.Ser212=)
c.4722A>C (p.Ser1574=)
c.4086A>C (p.Ser1362=)
c.876A>C (p.Ser292=)
5g.177260164A>GCA447726435NSD1c.4269A>G (p.Ser1423=)
n.4725A>G
c.4833A>G (p.Ser1611=)
n.4539A>G
n.5289A>G
c.5142A>G (p.Ser1714=)
c.4335A>G (p.Ser1445=)
c.636A>G (p.Ser212=)
c.4722A>G (p.Ser1574=)
c.4086A>G (p.Ser1362=)
c.876A>G (p.Ser292=)
5g.177260164A>TCA447726434NSD1c.4269A>T (p.Ser1423=)
n.4725A>T
c.4833A>T (p.Ser1611=)
n.4539A>T
n.5289A>T
c.5142A>T (p.Ser1714=)
c.4335A>T (p.Ser1445=)
c.636A>T (p.Ser212=)
c.4722A>T (p.Ser1574=)
c.4086A>T (p.Ser1362=)
c.876A>T (p.Ser292=)
dbSNP
5g.177260165G>ACA362303420NSD1c.4270G>A (p.Glu1424Lys)
n.4726G>A
c.4834G>A (p.Glu1612Lys)
n.4540G>A
n.5290G>A
c.5143G>A (p.Glu1715Lys)
c.4336G>A (p.Glu1446Lys)
c.637G>A (p.Glu213Lys)
c.4723G>A (p.Glu1575Lys)
c.4087G>A (p.Glu1363Lys)
c.877G>A (p.Glu293Lys)
5g.177260165G>CCA362303422NSD1c.4270G>C (p.Glu1424Gln)
n.4726G>C
c.4834G>C (p.Glu1612Gln)
n.4540G>C
n.5290G>C
c.5143G>C (p.Glu1715Gln)
c.4336G>C (p.Glu1446Gln)
c.637G>C (p.Glu213Gln)
c.4723G>C (p.Glu1575Gln)
c.4087G>C (p.Glu1363Gln)
c.877G>C (p.Glu293Gln)
5g.177260165G>TCA362303421NSD1c.4270G>T (p.Glu1424Ter)
n.4726G>T
c.4834G>T (p.Glu1612Ter)
n.4540G>T
n.5290G>T
c.5143G>T (p.Glu1715Ter)
c.4336G>T (p.Glu1446Ter)
c.637G>T (p.Glu213Ter)
c.4723G>T (p.Glu1575Ter)
c.4087G>T (p.Glu1363Ter)
c.877G>T (p.Glu293Ter)
ClinVar
5g.177260166A>CCA362303424NSD1c.4271A>C (p.Glu1424Ala)
n.4727A>C
c.4835A>C (p.Glu1612Ala)
n.4541A>C
n.5291A>C
c.5144A>C (p.Glu1715Ala)
c.4337A>C (p.Glu1446Ala)
c.638A>C (p.Glu213Ala)
c.4724A>C (p.Glu1575Ala)
c.4088A>C (p.Glu1363Ala)
c.878A>C (p.Glu293Ala)
5g.177260166A>GCA362303426NSD1c.4271A>G (p.Glu1424Gly)
n.4727A>G
c.4835A>G (p.Glu1612Gly)
n.4541A>G
n.5291A>G
c.5144A>G (p.Glu1715Gly)
c.4337A>G (p.Glu1446Gly)
c.638A>G (p.Glu213Gly)
c.4724A>G (p.Glu1575Gly)
c.4088A>G (p.Glu1363Gly)
c.878A>G (p.Glu293Gly)
5g.177260166A>TCA362303428NSD1c.4271A>T (p.Glu1424Val)
n.4727A>T
c.4835A>T (p.Glu1612Val)
n.4541A>T
n.5291A>T
c.5144A>T (p.Glu1715Val)
c.4337A>T (p.Glu1446Val)
c.638A>T (p.Glu213Val)
c.4724A>T (p.Glu1575Val)
c.4088A>T (p.Glu1363Val)
c.878A>T (p.Glu293Val)
5g.177260167A>CCA362303432NSD1c.4272A>C (p.Glu1424Asp)
n.4728A>C
c.4836A>C (p.Glu1612Asp)
n.4542A>C
n.5292A>C
c.5145A>C (p.Glu1715Asp)
c.4338A>C (p.Glu1446Asp)
c.639A>C (p.Glu213Asp)
c.4725A>C (p.Glu1575Asp)
c.4089A>C (p.Glu1363Asp)
c.879A>C (p.Glu293Asp)
5g.177260167A>GCA447726436NSD1c.4272A>G (p.Glu1424=)
n.4728A>G
c.4836A>G (p.Glu1612=)
n.4542A>G
n.5292A>G
c.5145A>G (p.Glu1715=)
c.4338A>G (p.Glu1446=)
c.639A>G (p.Glu213=)
c.4725A>G (p.Glu1575=)
c.4089A>G (p.Glu1363=)
c.879A>G (p.Glu293=)
COSMIC COSMIC
5g.177260167A>TCA362303433NSD1c.4272A>T (p.Glu1424Asp)
n.4728A>T
c.4836A>T (p.Glu1612Asp)
n.4542A>T
n.5292A>T
c.5145A>T (p.Glu1715Asp)
c.4338A>T (p.Glu1446Asp)
c.639A>T (p.Glu213Asp)
c.4725A>T (p.Glu1575Asp)
c.4089A>T (p.Glu1363Asp)
c.879A>T (p.Glu293Asp)
5g.177260168G>ACA362303436NSD1c.4273G>A (p.Gly1425Arg)
n.4729G>A
c.4837G>A (p.Gly1613Arg)
n.4543G>A
n.5293G>A
c.5146G>A (p.Gly1716Arg)
c.4339G>A (p.Gly1447Arg)
c.640G>A (p.Gly214Arg)
c.4726G>A (p.Gly1576Arg)
c.4090G>A (p.Gly1364Arg)
c.5146G>A (p.Asp1716Asn)
c.880G>A (p.Gly294Arg)
dbSNP
5g.177260168G>CCA362303438NSD1c.4273G>C (p.Gly1425Arg)
n.4729G>C
c.4837G>C (p.Gly1613Arg)
n.4543G>C
n.5293G>C
c.5146G>C (p.Gly1716Arg)
c.4339G>C (p.Gly1447Arg)
c.640G>C (p.Gly214Arg)
c.4726G>C (p.Gly1576Arg)
c.4090G>C (p.Gly1364Arg)
c.5146G>C (p.Asp1716His)
c.880G>C (p.Gly294Arg)
5g.177260168G>TCA362303439NSD1c.4273G>T (p.Gly1425Ter)
n.4729G>T
c.4837G>T (p.Gly1613Ter)
n.4543G>T
n.5293G>T
c.5146G>T (p.Gly1716Ter)
c.4339G>T (p.Gly1447Ter)
c.640G>T (p.Gly214Ter)
c.4726G>T (p.Gly1576Ter)
c.4090G>T (p.Gly1364Ter)
c.5146G>T (p.Asp1716Tyr)
c.880G>T (p.Gly294Ter)
5g.177260169G>ACA294939NSD1c.4273+1G>A (n.4273+1G>A)
n.4729+1G>A
c.4837+1G>A (n.4837+1G>A)
n.4543+1G>A
n.5293+1G>A
c.5146+1G>A (n.5146+1G>A)
c.4339+1G>A (n.4339+1G>A)
c.640+1G>A (n.640+1G>A)
c.4726+1G>A (n.4726+1G>A)
c.4090+1G>A (n.4090+1G>A)
c.880+1G>A (n.880+1G>A)
ClinVar dbSNP
5g.177260169G>CCA362303443NSD1c.4273+1G>C (n.4273+1G>C)
n.4729+1G>C
c.4837+1G>C (n.4837+1G>C)
n.4543+1G>C
n.5293+1G>C
c.5146+1G>C (n.5146+1G>C)
c.4339+1G>C (n.4339+1G>C)
c.640+1G>C (n.640+1G>C)
c.4726+1G>C (n.4726+1G>C)
c.4090+1G>C (n.4090+1G>C)
c.880+1G>C (n.880+1G>C)
5g.177260169G=CA1603527340NSD1c.4273+1G= (n.4273+1G=)
n.4729+1G=
c.4837+1G= (n.4837+1G=)
n.4543+1G=
n.5293+1G=
c.5146+1G= (n.5146+1G=)
c.4339+1G= (n.4339+1G=)
c.640+1G= (n.640+1G=)
c.4726+1G= (n.4726+1G=)
c.4090+1G= (n.4090+1G=)
c.880+1G= (n.880+1G=)
5g.177260169G>TCA362303445NSD1c.4273+1G>T (n.4273+1G>T)
n.4729+1G>T
c.4837+1G>T (n.4837+1G>T)
n.4543+1G>T
n.5293+1G>T
c.5146+1G>T (n.5146+1G>T)
c.4339+1G>T (n.4339+1G>T)
c.640+1G>T (n.640+1G>T)
c.4726+1G>T (n.4726+1G>T)
c.4090+1G>T (n.4090+1G>T)
c.880+1G>T (n.880+1G>T)
5g.177260170T>ACA362303451NSD1c.4273+2T>A (n.4273+2T>A)
n.4729+2T>A
c.4837+2T>A (n.4837+2T>A)
n.4543+2T>A
n.5293+2T>A
c.5146+2T>A (n.5146+2T>A)
c.4339+2T>A (n.4339+2T>A)
c.640+2T>A (n.640+2T>A)
c.4726+2T>A (n.4726+2T>A)
c.4090+2T>A (n.4090+2T>A)
c.880+2T>A (n.880+2T>A)
5g.177260170T>CCA362303453NSD1c.4273+2T>C (n.4273+2T>C)
n.4729+2T>C
c.4837+2T>C (n.4837+2T>C)
n.4543+2T>C
n.5293+2T>C
c.5146+2T>C (n.5146+2T>C)
c.4339+2T>C (n.4339+2T>C)
c.640+2T>C (n.640+2T>C)
c.4726+2T>C (n.4726+2T>C)
c.4090+2T>C (n.4090+2T>C)
c.880+2T>C (n.880+2T>C)
5g.177260170T>GCA362303447NSD1c.4273+2T>G (n.4273+2T>G)
n.4729+2T>G
c.4837+2T>G (n.4837+2T>G)
n.4543+2T>G
n.5293+2T>G
c.5146+2T>G (n.5146+2T>G)
c.4339+2T>G (n.4339+2T>G)
c.640+2T>G (n.640+2T>G)
c.4726+2T>G (n.4726+2T>G)
c.4090+2T>G (n.4090+2T>G)
c.880+2T>G (n.880+2T>G)
gnomAD v4
5g.177260170dupCA915942756NSD1c.4273+2dup (n.4273+2dup)
n.4729+2dup
c.4837+2dup (n.4837+2dup)
n.4543+2dup
n.5293+2dup
c.5146+2dup (n.5146+2dup)
c.4339+2dup (n.4339+2dup)
c.640+2dup (n.640+2dup)
c.4726+2dup (n.4726+2dup)
c.4090+2dup (n.4090+2dup)
c.880+2dup (n.880+2dup)
ClinVar dbSNP
5g.177260172A=CA1603527360NSD1c.4273+4A= (n.4273+4A=)
n.4729+4A=
c.4837+4A= (n.4837+4A=)
n.4543+4A=
n.5293+4A=
c.5146+4A= (n.5146+4A=)
c.4339+4A= (n.4339+4A=)
c.640+4A= (n.640+4A=)
c.4726+4A= (n.4726+4A=)
c.4090+4A= (n.4090+4A=)
c.880+4A= (n.880+4A=)
5g.177260172A>GCA3577768NSD1c.4273+4A>G (n.4273+4A>G)
n.4729+4A>G
c.4837+4A>G (n.4837+4A>G)
n.4543+4A>G
n.5293+4A>G
c.5146+4A>G (n.5146+4A>G)
c.4339+4A>G (n.4339+4A>G)
c.640+4A>G (n.640+4A>G)
c.4726+4A>G (n.4726+4A>G)
c.4090+4A>G (n.4090+4A>G)
c.880+4A>G (n.880+4A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177260177T>CCA3577769NSD1c.4273+9T>C (n.4273+9T>C)
n.4729+9T>C
c.4837+9T>C (n.4837+9T>C)
n.4543+9T>C
n.5293+9T>C
c.5146+9T>C (n.5146+9T>C)
c.4339+9T>C (n.4339+9T>C)
c.640+9T>C (n.640+9T>C)
c.4726+9T>C (n.4726+9T>C)
c.4090+9T>C (n.4090+9T>C)
c.880+9T>C (n.880+9T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177260177T=CA1603527367NSD1c.4273+9T= (n.4273+9T=)
n.4729+9T=
c.4837+9T= (n.4837+9T=)
n.4543+9T=
n.5293+9T=
c.5146+9T= (n.5146+9T=)
c.4339+9T= (n.4339+9T=)
c.640+9T= (n.640+9T=)
c.4726+9T= (n.4726+9T=)
c.4090+9T= (n.4090+9T=)
c.880+9T= (n.880+9T=)
5g.177260178delCA2676689661NSD1c.4273+10del (n.4273+10del)
n.4729+10del
c.4837+10del (n.4837+10del)
n.4543+10del
n.5293+10del
c.5146+10del (n.5146+10del)
c.4339+10del (n.4339+10del)
c.640+10del (n.640+10del)
c.4726+10del (n.4726+10del)
c.4090+10del (n.4090+10del)
c.880+10del (n.880+10del)
gnomAD v4
5g.177260178C>GCA2578494960NSD1c.4273+10C>G (n.4273+10C>G)
n.4729+10C>G
c.4837+10C>G (n.4837+10C>G)
n.4543+10C>G
n.5293+10C>G
c.5146+10C>G (n.5146+10C>G)
c.4339+10C>G (n.4339+10C>G)
c.640+10C>G (n.640+10C>G)
c.4726+10C>G (n.4726+10C>G)
c.4090+10C>G (n.4090+10C>G)
c.880+10C>G (n.880+10C>G)
gnomAD v4
5g.177260180T>GCA564899147NSD1c.4273+12T>G (n.4273+12T>G)
n.4729+12T>G
c.4837+12T>G (n.4837+12T>G)
n.4543+12T>G
n.5293+12T>G
c.5146+12T>G (n.5146+12T>G)
c.4339+12T>G (n.4339+12T>G)
c.640+12T>G (n.640+12T>G)
c.4726+12T>G (n.4726+12T>G)
c.4090+12T>G (n.4090+12T>G)
c.880+12T>G (n.880+12T>G)
dbSNP gnomAD v2
5g.177260180T=CA1603527373NSD1c.4273+12T= (n.4273+12T=)
n.4729+12T=
c.4837+12T= (n.4837+12T=)
n.4543+12T=
n.5293+12T=
c.5146+12T= (n.5146+12T=)
c.4339+12T= (n.4339+12T=)
c.640+12T= (n.640+12T=)
c.4726+12T= (n.4726+12T=)
c.4090+12T= (n.4090+12T=)
c.880+12T= (n.880+12T=)
5g.177260180_177260183delinsTTTCCA1603527376NSD1c.4273+12_4273+15delinsTTTC (n.4273+12_4273+15delinsTTTC)
n.4729+12_4729+15delinsTTTC
c.4837+12_4837+15delinsTTTC (n.4837+12_4837+15delinsTTTC)
n.4543+12_4543+15delinsTTTC
n.5293+12_5293+15delinsTTTC
c.5146+12_5146+15delinsTTTC (n.5146+12_5146+15delinsTTTC)
c.4339+12_4339+15delinsTTTC (n.4339+12_4339+15delinsTTTC)
c.640+12_640+15delinsTTTC (n.640+12_640+15delinsTTTC)
c.4726+12_4726+15delinsTTTC (n.4726+12_4726+15delinsTTTC)
c.4090+12_4090+15delinsTTTC (n.4090+12_4090+15delinsTTTC)
c.880+12_880+15delinsTTTC (n.880+12_880+15delinsTTTC)
5g.177260184_177260186delCA1603527379NSD1c.4273+16_4273+18del (n.4273+16_4273+18del)
n.4729+16_4729+18del
c.4837+16_4837+18del (n.4837+16_4837+18del)
n.4543+16_4543+18del
n.5293+16_5293+18del
c.5146+16_5146+18del (n.5146+16_5146+18del)
c.4339+16_4339+18del (n.4339+16_4339+18del)
c.640+16_640+18del (n.640+16_640+18del)
c.4726+16_4726+18del (n.4726+16_4726+18del)
c.4090+16_4090+18del (n.4090+16_4090+18del)
c.880+16_880+18del (n.880+16_880+18del)
dbSNP gnomAD v4

Number of alleles fetched