Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154928667_154928668delinsCGCA2466835761F8c.5122_5123delinsCG (p.Arg1708=)
c.5017_5018delinsCG (p.Arg1673=)
Xg.154928668G>ACA120919F8c.5122C>T (p.Arg1708Cys)
c.5017C>T (p.Arg1673Cys)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.154928668G>CCA414913845F8c.5122C>G (p.Arg1708Gly)
c.5017C>G (p.Arg1673Gly)
Xg.154928668G=CA2466835762F8c.5122C= (p.Arg1708=)
c.5017C= (p.Arg1673=)
Xg.154928668G>TCA414913844F8c.5122C>A (p.Arg1708Ser)
c.5017C>A (p.Arg1673Ser)
dbSNP
Xg.154928672delCA873340216F8c.5122del (p.Arg1708AlafsTer23)
c.5017del (p.Arg1673AlafsTer23)
dbSNP
Xg.154928669G>ACA519718380F8c.5121C>T (p.Pro1707=)
c.5016C>T (p.Pro1672=)
Xg.154928669G>CCA519718381F8c.5121C>G (p.Pro1707=)
c.5016C>G (p.Pro1672=)
Xg.154928669G>TCA519718382F8c.5121C>A (p.Pro1707=)
c.5016C>A (p.Pro1672=)
gnomAD v4
Xg.154928670G>ACA10568036F8c.5120C>T (p.Pro1707Leu)
c.5015C>T (p.Pro1672Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154928670G>CCA414913848F8c.5120C>G (p.Pro1707Arg)
c.5015C>G (p.Pro1672Arg)
Xg.154928670G=CA2466835763F8c.5120C= (p.Pro1707=)
c.5015C= (p.Pro1672=)
Xg.154928670G>TCA414913847F8c.5120C>A (p.Pro1707His)
c.5015C>A (p.Pro1672His)
Xg.154928671G>ACA414913850F8c.5119C>T (p.Pro1707Ser)
c.5014C>T (p.Pro1672Ser)
Xg.154928671G>CCA414913853F8c.5119C>G (p.Pro1707Ala)
c.5014C>G (p.Pro1672Ala)
Xg.154928671G>TCA414913851F8c.5119C>A (p.Pro1707Thr)
c.5014C>A (p.Pro1672Thr)
Xg.154928672G>ACA519718383F8c.5118C>T (p.Ser1706=)
c.5013C>T (p.Ser1671=)
gnomAD v4
Xg.154928672G>CCA414913854F8c.5118C>G (p.Ser1706Arg)
c.5013C>G (p.Ser1671Arg)
Xg.154928672G>TCA414913856F8c.5118C>A (p.Ser1706Arg)
c.5013C>A (p.Ser1671Arg)
gnomAD v4
Xg.154928673C>ACA10568037F8c.5117G>T (p.Ser1706Ile)
c.5012G>T (p.Ser1671Ile)
dbSNP ExAC
Xg.154928673C=CA2466835764F8c.5117G= (p.Ser1706=)
c.5012G= (p.Ser1671=)
Xg.154928673C>GCA414913858F8c.5117G>C (p.Ser1706Thr)
c.5012G>C (p.Ser1671Thr)
Xg.154928673C>TCA414913860F8c.5117G>A (p.Ser1706Asn)
c.5012G>A (p.Ser1671Asn)
gnomAD v4
Xg.154928674T>ACA414913862F8c.5116A>T (p.Ser1706Cys)
c.5011A>T (p.Ser1671Cys)
Xg.154928674T>CCA414913864F8c.5116A>G (p.Ser1706Gly)
c.5011A>G (p.Ser1671Gly)
Xg.154928674T>GCA414913865F8c.5116A>C (p.Ser1706Arg)
c.5011A>C (p.Ser1671Arg)
Xg.154928675C>ACA414913867F8c.5115G>T (p.Gln1705His)
c.5010G>T (p.Gln1670His)
Xg.154928675C>GCA414913869F8c.5115G>C (p.Gln1705His)
c.5010G>C (p.Gln1670His)
Xg.154928675C>TCA519718384F8c.5115G>A (p.Gln1705=)
c.5010G>A (p.Gln1670=)
Xg.154928676delCA2695237918F8c.5114del (p.Gln1705ArgfsTer26)
c.5009del (p.Gln1670ArgfsTer26)
Xg.154928676T>ACA414913874F8c.5114A>T (p.Gln1705Leu)
c.5009A>T (p.Gln1670Leu)
Xg.154928676T>CCA414913872F8c.5114A>G (p.Gln1705Arg)
c.5009A>G (p.Gln1670Arg)
Xg.154928676T>GCA414913871F8c.5114A>C (p.Gln1705Pro)
c.5009A>C (p.Gln1670Pro)
Xg.154928677G>ACA255020F8c.5113C>T (p.Gln1705Ter)
c.5008C>T (p.Gln1670Ter)
ClinVar dbSNP
Xg.154928677G>CCA414913877F8c.5113C>G (p.Gln1705Glu)
c.5008C>G (p.Gln1670Glu)
dbSNP gnomAD v2 gnomAD v4
Xg.154928677G=CA2466835765F8c.5113C= (p.Gln1705=)
c.5008C= (p.Gln1670=)
Xg.154928677G>TCA414913878F8c.5113C>A (p.Gln1705Lys)
c.5008C>A (p.Gln1670Lys)
Xg.154928677_154928678dupCA2695237921F8c.5112_5113dup (p.Gln1705LeufsTer27)
c.5007_5008dup (p.Gln1670LeufsTer27)
Xg.154928678A=CA2466835766F8c.5112T= (p.Asn1704=)
c.5007T= (p.Asn1669=)
Xg.154928678A>CCA414913880F8c.5112T>G (p.Asn1704Lys)
c.5007T>G (p.Asn1669Lys)
gnomAD v4
Xg.154928678A>GCA519718385F8c.5112T>C (p.Asn1704=)
c.5007T>C (p.Asn1669=)
Xg.154928678A>TCA414913882F8c.5112T>A (p.Asn1704Lys)
c.5007T>A (p.Asn1669Lys)
Xg.154928679T>ACA414913884F8c.5111A>T (p.Asn1704Ile)
c.5006A>T (p.Asn1669Ile)
Xg.154928679T>CCA414913886F8c.5111A>G (p.Asn1704Ser)
c.5006A>G (p.Asn1669Ser)
Xg.154928679T>GCA414913887F8c.5111A>C (p.Asn1704Thr)
c.5006A>C (p.Asn1669Thr)
Xg.154928681_154928682dupCA873340243F8c.5110_5111dup (p.Asn1704LysfsTer28)
c.5005_5006dup (p.Asn1669LysfsTer28)
dbSNP
Xg.154928682delCA2695237923F8c.5111del (p.Asn1704IlefsTer27)
c.5006del (p.Asn1669IlefsTer27)
Xg.154928680T>ACA414913889F8c.5110A>T (p.Asn1704Tyr)
c.5005A>T (p.Asn1669Tyr)
Xg.154928680T>CCA414913891F8c.5110A>G (p.Asn1704Asp)
c.5005A>G (p.Asn1669Asp)
Xg.154928680T>GCA414913893F8c.5110A>C (p.Asn1704His)
c.5005A>C (p.Asn1669His)

Number of alleles fetched