Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.855969C>ACA504686342ELANEc.609C>A (p.Gly203=)
19g.855969C>GCA504686340ELANEc.609C>G (p.Gly203=)
19g.855969C>TCA504686337ELANEc.609C>T (p.Gly203=)
19g.855970A>CCA402918885ELANEc.610A>C (p.Ser204Arg)
19g.855970A>GCA402918887ELANEc.610A>G (p.Ser204Gly)
gnomAD v4
19g.855970A>TCA402918884ELANEc.610A>T (p.Ser204Cys)
19g.855971G>ACA402918889ELANEc.611G>A (p.Ser204Asn)
COSMIC
19g.855971G>CCA402918890ELANEc.611G>C (p.Ser204Thr)
19g.855971G>TCA402918892ELANEc.611G>T (p.Ser204Ile)
19g.855972C>ACA402918894ELANEc.612C>A (p.Ser204Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855972C=CA2317361605ELANEc.612C= (p.Ser204=)
19g.855972C>GCA402918896ELANEc.612C>G (p.Ser204Arg)
19g.855972C>TCA9026121ELANEc.612C>T (p.Ser204=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855975delCA2695227814ELANEc.615del (p.Leu206TrpfsTer6)
19g.855973C>ACA402918897ELANEc.613C>A (p.Pro205Thr)
19g.855973C=CA2317361606ELANEc.613C= (p.Pro205=)
19g.855973C>GCA402918901ELANEc.613C>G (p.Pro205Ala)
dbSNP gnomAD v2 gnomAD v4
19g.855973C>TCA402918898ELANEc.613C>T (p.Pro205Ser)
19g.855974C>ACA402918903ELANEc.614C>A (p.Pro205His)
19g.855974C=CA2317361607ELANEc.614C= (p.Pro205=)
19g.855974C>GCA402918904ELANEc.614C>G (p.Pro205Arg)
ClinVar dbSNP
19g.855974C>TCA402918906ELANEc.614C>T (p.Pro205Leu)
19g.855975C>ACA504686369ELANEc.615C>A (p.Pro205=)
19g.855975C>GCA504686371ELANEc.615C>G (p.Pro205=)
19g.855975C>TCA504686372ELANEc.615C>T (p.Pro205=)
gnomAD v4
19g.855975_855978delCA2695227815ELANEc.615_618del (p.Leu206SerfsTer5)
19g.855976T>ACA402918908ELANEc.616T>A (p.Leu206Met)
19g.855976T>CCA504686378ELANEc.616T>C (p.Leu206=)
gnomAD v4
19g.855976T>GCA402918910ELANEc.616T>G (p.Leu206Val)
19g.855977T>ACA402918914ELANEc.617T>A (p.Leu206Ter)
19g.855977T>CCA402918915ELANEc.617T>C (p.Leu206Ser)
19g.855977T>GCA402918912ELANEc.617T>G (p.Leu206Trp)
19g.855978G>ACA504686387ELANEc.618G>A (p.Leu206=)
ClinVar
19g.855978G>CCA402918918ELANEc.618G>C (p.Leu206Phe)
ClinVar dbSNP
19g.855978G=CA2317361608ELANEc.618G= (p.Leu206=)
19g.855978G>TCA281046ELANEc.618G>T (p.Leu206Phe)
ClinVar dbSNP
19g.855979G>ACA402918920ELANEc.619G>A (p.Val207Ile)
gnomAD v4 COSMIC
19g.855979G>CCA402918921ELANEc.619G>C (p.Val207Leu)
ClinVar dbSNP gnomAD v4
19g.855979G=CA2317361609ELANEc.619G= (p.Val207=)
19g.855979G>TCA402918924ELANEc.619G>T (p.Val207Phe)
ClinVar dbSNP
19g.855980T>ACA402918926ELANEc.620T>A (p.Val207Asp)
19g.855980T>CCA402918927ELANEc.620T>C (p.Val207Ala)
dbSNP
19g.855980T>GCA402918929ELANEc.620T>G (p.Val207Gly)
19g.855981C>ACA504686406ELANEc.621C>A (p.Val207=)
19g.855981C=CA2317361610ELANEc.621C= (p.Val207=)
19g.855981C>GCA504686408ELANEc.621C>G (p.Val207=)
dbSNP gnomAD v3 gnomAD v4
19g.855981C>TCA504686410ELANEc.621C>T (p.Val207=)
gnomAD v4
19g.855982T>ACA402918931ELANEc.622T>A (p.Cys208Ser)
19g.855982T>CCA402918932ELANEc.622T>C (p.Cys208Arg)
19g.855982T>GCA402918933ELANEc.622T>G (p.Cys208Gly)
ClinVar dbSNP

Number of alleles fetched