Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.173908360_173915405delCA2573051419SERPINC1c.42-486_1154-846del
c.42-486_560-867del
c.-272-219_1010-846del
c.42-486_1277-846del
c.123-486_1235-846del
c.42-486_1133-846del
c.42-486_1097-846del
c.42-486_938-846del
ClinVar
1g.173910345_173913622delCA2573051421SERPINC1c.408+948_763-386del
n.113+948_414-386del
c.408+948_559+1536del
c.264+948_619-386del
c.408+948_885+303del
c.489+948_844-386del
c.408+948_742-386del
c.408+948_762+426del
c.408+948_547-386del
ClinVar
1g.173911379_173915115delCA2573051422SERPINC1c.42-196_624+420del
c.42-196_559+485del
c.-201_480+420del
c.123-196_705+420del
c.42-196_409-488del
1g.173911749_173917428delCA1139655524 ClinVar
1g.173911889A>CCA421823021SERPINC1c.534T>G (p.Leu178=)
n.239T>G
c.390T>G (p.Leu130=)
c.615T>G (p.Leu205=)
c.409-998T>G (n.409-998T>G)
1g.173911889A>GCA421823023SERPINC1c.534T>C (p.Leu178=)
n.239T>C
c.390T>C (p.Leu130=)
c.615T>C (p.Leu205=)
c.409-998T>C (n.409-998T>C)
1g.173911889A>TCA421823024SERPINC1c.534T>A (p.Leu178=)
n.239T>A
c.390T>A (p.Leu130=)
c.615T>A (p.Leu205=)
c.409-998T>A (n.409-998T>A)
1g.173911890A>CCA343776475SERPINC1c.533T>G (p.Leu178Arg)
n.238T>G
c.389T>G (p.Leu130Arg)
c.614T>G (p.Leu205Arg)
c.409-999T>G (n.409-999T>G)
COSMIC
1g.173911890A>GCA343776476SERPINC1c.533T>C (p.Leu178Pro)
n.238T>C
c.389T>C (p.Leu130Pro)
c.614T>C (p.Leu205Pro)
c.409-999T>C (n.409-999T>C)
1g.173911890A>TCA343776478SERPINC1c.533T>A (p.Leu178His)
n.238T>A
c.389T>A (p.Leu130His)
c.614T>A (p.Leu205His)
c.409-999T>A (n.409-999T>A)
1g.173911891G>ACA343776479SERPINC1c.532C>T (p.Leu178Phe)
n.237C>T
c.388C>T (p.Leu130Phe)
c.613C>T (p.Leu205Phe)
c.409-1000C>T (n.409-1000C>T)
gnomAD v4
1g.173911891G>CCA343776481SERPINC1c.532C>G (p.Leu178Val)
n.237C>G
c.388C>G (p.Leu130Val)
c.613C>G (p.Leu205Val)
c.409-1000C>G (n.409-1000C>G)
1g.173911891G>TCA343776480SERPINC1c.532C>A (p.Leu178Ile)
n.237C>A
c.388C>A (p.Leu130Ile)
c.613C>A (p.Leu205Ile)
c.409-1000C>A (n.409-1000C>A)
1g.173911892G>ACA421823028SERPINC1c.531C>T (p.Arg177=)
n.236C>T
c.387C>T (p.Arg129=)
c.612C>T (p.Arg204=)
c.409-1001C>T (n.409-1001C>T)
1g.173911892G>CCA421823027SERPINC1c.531C>G (p.Arg177=)
n.236C>G
c.387C>G (p.Arg129=)
c.612C>G (p.Arg204=)
c.409-1001C>G (n.409-1001C>G)
1g.173911892G>TCA421823026SERPINC1c.531C>A (p.Arg177=)
n.236C>A
c.387C>A (p.Arg129=)
c.612C>A (p.Arg204=)
c.409-1001C>A (n.409-1001C>A)
1g.173911893C>ACA343776483SERPINC1c.530G>T (p.Arg177Leu)
n.235G>T
c.386G>T (p.Arg129Leu)
c.611G>T (p.Arg204Leu)
c.409-1002G>T (n.409-1002G>T)
dbSNP
1g.173911893C=CA1207937819SERPINC1c.530G= (p.Arg177=)
n.235G=
c.386G= (p.Arg129=)
c.611G= (p.Arg204=)
c.409-1002G= (n.409-1002G=)
1g.173911893C>GCA343776484SERPINC1c.530G>C (p.Arg177Pro)
n.235G>C
c.386G>C (p.Arg129Pro)
c.611G>C (p.Arg204Pro)
c.409-1002G>C (n.409-1002G>C)
1g.173911893C>TCA10581757SERPINC1c.530G>A (p.Arg177His)
n.235G>A
c.386G>A (p.Arg129His)
c.611G>A (p.Arg204His)
c.409-1002G>A (n.409-1002G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.173911894G>ACA1251403SERPINC1c.529C>T (p.Arg177Cys)
n.234C>T
c.385C>T (p.Arg129Cys)
c.610C>T (p.Arg204Cys)
c.409-1003C>T (n.409-1003C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.173911894G>CCA343776487SERPINC1c.529C>G (p.Arg177Gly)
n.234C>G
c.385C>G (p.Arg129Gly)
c.610C>G (p.Arg204Gly)
c.409-1003C>G (n.409-1003C>G)
1g.173911894G=CA1141934734SERPINC1c.529C= (p.Arg177=)
n.234C=
c.385C= (p.Arg129=)
c.610C= (p.Arg204=)
c.409-1003C= (n.409-1003C=)
1g.173911894G>TCA343776489SERPINC1c.529C>A (p.Arg177Ser)
n.234C>A
c.385C>A (p.Arg129Ser)
c.610C>A (p.Arg204Ser)
c.409-1003C>A (n.409-1003C>A)
dbSNP gnomAD v3 gnomAD v4
1g.173911895A=CA1207937820SERPINC1c.528T= (p.Asn176=)
n.233T=
c.384T= (p.Asn128=)
c.609T= (p.Asn203=)
c.409-1004T= (n.409-1004T=)
1g.173911895A>CCA343776490SERPINC1c.528T>G (p.Asn176Lys)
n.233T>G
c.384T>G (p.Asn128Lys)
c.609T>G (p.Asn203Lys)
c.409-1004T>G (n.409-1004T>G)
1g.173911895A>GCA421823032SERPINC1c.528T>C (p.Asn176=)
n.233T>C
c.384T>C (p.Asn128=)
c.609T>C (p.Asn203=)
c.409-1004T>C (n.409-1004T>C)
dbSNP
1g.173911895A>TCA343776492SERPINC1c.528T>A (p.Asn176Lys)
n.233T>A
c.384T>A (p.Asn128Lys)
c.609T>A (p.Asn203Lys)
c.409-1004T>A (n.409-1004T>A)
1g.173911896T>ACA343776495SERPINC1c.527A>T (p.Asn176Ile)
n.232A>T
c.383A>T (p.Asn128Ile)
c.608A>T (p.Asn203Ile)
c.409-1005A>T (n.409-1005A>T)
1g.173911896T>CCA343776496SERPINC1c.527A>G (p.Asn176Ser)
n.232A>G
c.383A>G (p.Asn128Ser)
c.608A>G (p.Asn203Ser)
c.409-1005A>G (n.409-1005A>G)
dbSNP
1g.173911896T>GCA343776497SERPINC1c.527A>C (p.Asn176Thr)
n.232A>C
c.383A>C (p.Asn128Thr)
c.608A>C (p.Asn203Thr)
c.409-1005A>C (n.409-1005A>C)
1g.173911896T=CA1207937821SERPINC1c.527A= (p.Asn176=)
n.232A=
c.383A= (p.Asn128=)
c.608A= (p.Asn203=)
c.409-1005A= (n.409-1005A=)
1g.173911897T>ACA343776502SERPINC1c.526A>T (p.Asn176Tyr)
n.231A>T
c.382A>T (p.Asn128Tyr)
c.607A>T (p.Asn203Tyr)
c.409-1006A>T (n.409-1006A>T)
1g.173911897T>CCA343776501SERPINC1c.526A>G (p.Asn176Asp)
n.231A>G
c.382A>G (p.Asn128Asp)
c.607A>G (p.Asn203Asp)
c.409-1006A>G (n.409-1006A>G)
1g.173911897T>GCA343776499SERPINC1c.526A>C (p.Asn176His)
n.231A>C
c.382A>C (p.Asn128His)
c.607A>C (p.Asn203His)
c.409-1006A>C (n.409-1006A>C)
1g.173911898G>ACA421823035SERPINC1c.525C>T (p.Ala175=)
n.230C>T
c.381C>T (p.Ala127=)
c.606C>T (p.Ala202=)
c.409-1007C>T (n.409-1007C>T)
ClinVar dbSNP gnomAD v4
1g.173911898G>CCA421823036SERPINC1c.525C>G (p.Ala175=)
n.230C>G
c.381C>G (p.Ala127=)
c.606C>G (p.Ala202=)
c.409-1007C>G (n.409-1007C>G)
1g.173911898G=CA1207937822SERPINC1c.525C= (p.Ala175=)
n.230C=
c.381C= (p.Ala127=)
c.606C= (p.Ala202=)
c.409-1007C= (n.409-1007C=)
1g.173911898G>TCA421823037SERPINC1c.525C>A (p.Ala175=)
n.230C>A
c.381C>A (p.Ala127=)
c.606C>A (p.Ala202=)
c.409-1007C>A (n.409-1007C>A)
1g.173911899G>ACA343776504SERPINC1c.524C>T (p.Ala175Val)
n.229C>T
c.380C>T (p.Ala127Val)
c.605C>T (p.Ala202Val)
c.409-1008C>T (n.409-1008C>T)
1g.173911899G>CCA343776506SERPINC1c.524C>G (p.Ala175Gly)
n.229C>G
c.380C>G (p.Ala127Gly)
c.605C>G (p.Ala202Gly)
c.409-1008C>G (n.409-1008C>G)
1g.173911899G>TCA343776507SERPINC1c.524C>A (p.Ala175Asp)
n.229C>A
c.380C>A (p.Ala127Asp)
c.605C>A (p.Ala202Asp)
c.409-1008C>A (n.409-1008C>A)
1g.173911900C>ACA343776509SERPINC1c.523G>T (p.Ala175Ser)
n.228G>T
c.379G>T (p.Ala127Ser)
c.604G>T (p.Ala202Ser)
c.409-1009G>T (n.409-1009G>T)
1g.173911900C=CA1207937823SERPINC1c.523G= (p.Ala175=)
n.228G=
c.379G= (p.Ala127=)
c.604G= (p.Ala202=)
c.409-1009G= (n.409-1009G=)
1g.173911900C>GCA343776511SERPINC1c.523G>C (p.Ala175Pro)
n.228G>C
c.379G>C (p.Ala127Pro)
c.604G>C (p.Ala202Pro)
c.409-1009G>C (n.409-1009G>C)
1g.173911900C>TCA343776513SERPINC1c.523G>A (p.Ala175Thr)
n.228G>A
c.379G>A (p.Ala127Thr)
c.604G>A (p.Ala202Thr)
c.409-1009G>A (n.409-1009G>A)
dbSNP gnomAD v2 gnomAD v4
1g.173911901T>ACA421823042SERPINC1c.522A>T (p.Ser174=)
n.227A>T
c.378A>T (p.Ser126=)
c.603A>T (p.Ser201=)
c.409-1010A>T (n.409-1010A>T)
1g.173911901T>CCA421823043SERPINC1c.522A>G (p.Ser174=)
n.227A>G
c.378A>G (p.Ser126=)
c.603A>G (p.Ser201=)
c.409-1010A>G (n.409-1010A>G)
dbSNP gnomAD v3 gnomAD v4
1g.173911901T>GCA421823044SERPINC1c.522A>C (p.Ser174=)
n.227A>C
c.378A>C (p.Ser126=)
c.603A>C (p.Ser201=)
c.409-1010A>C (n.409-1010A>C)
1g.173911902G>ACA343776519SERPINC1c.521C>T (p.Ser174Leu)
n.226C>T
c.377C>T (p.Ser126Leu)
c.602C>T (p.Ser201Leu)
c.409-1011C>T (n.409-1011C>T)

Number of alleles fetched