Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.17065531T>ACA376154193CUBNc.3116A>T (p.Tyr1039Phe)
10g.17065531T>CCA5424761CUBNc.3116A>G (p.Tyr1039Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.17065531T>GCA376154196CUBNc.3116A>C (p.Tyr1039Ser)
dbSNP gnomAD v4
10g.17065531T=CA1893442243CUBNc.3116A= (p.Tyr1039=)
10g.17065532A>CCA376154206CUBNc.3115T>G (p.Tyr1039Asp)
10g.17065532A>GCA376154202CUBNc.3115T>C (p.Tyr1039His)
gnomAD v4
10g.17065532A>TCA376154200CUBNc.3115T>A (p.Tyr1039Asn)
10g.17065533G>ACA468302676CUBNc.3114C>T (p.Asn1038=)
10g.17065533G>CCA376154208CUBNc.3114C>G (p.Asn1038Lys)
10g.17065533G>TCA376154210CUBNc.3114C>A (p.Asn1038Lys)
10g.17065534T>ACA376154212CUBNc.3113A>T (p.Asn1038Ile)
10g.17065534T>CCA376154215CUBNc.3113A>G (p.Asn1038Ser)
10g.17065534T>GCA376154218CUBNc.3113A>C (p.Asn1038Thr)
10g.17065535T>ACA376154219CUBNc.3112A>T (p.Asn1038Tyr)
10g.17065535T>CCA376154221CUBNc.3112A>G (p.Asn1038Asp)
COSMIC
10g.17065535T>GCA376154222CUBNc.3112A>C (p.Asn1038His)
10g.17065536T>ACA468302678CUBNc.3111A>T (p.Ile1037=)
10g.17065536T>CCA376154225CUBNc.3111A>G (p.Ile1037Met)
gnomAD v4
10g.17065536T>GCA468302677CUBNc.3111A>C (p.Ile1037=)
10g.17065537A>CCA376154227CUBNc.3110T>G (p.Ile1037Arg)
10g.17065537A>GCA376154229CUBNc.3110T>C (p.Ile1037Thr)
COSMIC
10g.17065537A>TCA376154230CUBNc.3110T>A (p.Ile1037Lys)
10g.17065538T>ACA376154233CUBNc.3109A>T (p.Ile1037Leu)
10g.17065538T>CCA376154236CUBNc.3109A>G (p.Ile1037Val)
10g.17065538T>GCA376154237CUBNc.3109A>C (p.Ile1037Leu)
10g.17065539T>ACA376154240CUBNc.3108A>T (p.Leu1036Phe)
10g.17065539T>CCA468302679CUBNc.3108A>G (p.Leu1036=)
10g.17065539T>GCA376154243CUBNc.3108A>C (p.Leu1036Phe)
10g.17065540A>CCA376154247CUBNc.3107T>G (p.Leu1036Ter)
10g.17065540A>GCA376154249CUBNc.3107T>C (p.Leu1036Ser)
10g.17065540A>TCA376154251CUBNc.3107T>A (p.Leu1036Ter)
10g.17065541A>CCA376154255CUBNc.3106T>G (p.Leu1036Val)
10g.17065541A>GCA468302680CUBNc.3106T>C (p.Leu1036=)
10g.17065541A>TCA376154257CUBNc.3106T>A (p.Leu1036Ile)
10g.17065542G>ACA468302681CUBNc.3105C>T (p.Phe1035=)
ClinVar dbSNP
10g.17065542G>CCA376154260CUBNc.3105C>G (p.Phe1035Leu)
10g.17065542G>TCA376154262CUBNc.3105C>A (p.Phe1035Leu)
10g.17065543A>CCA376154264CUBNc.3104T>G (p.Phe1035Cys)
10g.17065543A>GCA376154267CUBNc.3104T>C (p.Phe1035Ser)
gnomAD v4
10g.17065543A>TCA376154270CUBNc.3104T>A (p.Phe1035Tyr)
10g.17065544A>CCA376154273CUBNc.3103T>G (p.Phe1035Val)
10g.17065544A>GCA376154276CUBNc.3103T>C (p.Phe1035Leu)
gnomAD v4
10g.17065544A>TCA376154279CUBNc.3103T>A (p.Phe1035Ile)
10g.17065545G>ACA468302682CUBNc.3102C>T (p.Gly1034=)
dbSNP gnomAD v3 gnomAD v4
10g.17065545G>CCA468302683CUBNc.3102C>G (p.Gly1034=)
10g.17065545G=CA1893442244CUBNc.3102C= (p.Gly1034=)
10g.17065545G>TCA468302684CUBNc.3102C>A (p.Gly1034=)
10g.17065546C>ACA376154287CUBNc.3101G>T (p.Gly1034Val)
gnomAD v4 COSMIC
10g.17065546C=CA1893442245CUBNc.3101G= (p.Gly1034=)
10g.17065546C>GCA5424762CUBNc.3101G>C (p.Gly1034Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched