Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128849374G>A | CA166185381 | FLNC | c.4995G>A (p.Val1665=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128849374G>C | CA457849011 | FLNC | c.4995G>C (p.Val1665=) | |
7 | g.128849374G= | CA1742564274 | FLNC | c.4995G= (p.Val1665=) | |
7 | g.128849374G>T | CA457849012 | FLNC | c.4995G>T (p.Val1665=) | |
7 | g.128849375A= | CA1742564284 | FLNC | c.4996A= (p.Ile1666=) | |
7 | g.128849375A>C | CA369203953 | FLNC | c.4996A>C (p.Ile1666Leu) | |
7 | g.128849375A>G | CA369203954 | FLNC | c.4996A>G (p.Ile1666Val) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128849375A>T | CA369203955 | FLNC | c.4996A>T (p.Ile1666Phe) | |
7 | g.128849376T>A | CA369203956 | FLNC | c.4997T>A (p.Ile1666Asn) | |
7 | g.128849376T>C | CA369203957 | FLNC | c.4997T>C (p.Ile1666Thr) | |
7 | g.128849376T>G | CA369203958 | FLNC | c.4997T>G (p.Ile1666Ser) | |
7 | g.128849377C>A | CA457849017 | FLNC | c.4998C>A (p.Ile1666=) | |
7 | g.128849377C= | CA1742564289 | FLNC | c.4998C= (p.Ile1666=) | |
7 | g.128849377C>G | CA369203959 | FLNC | c.4998C>G (p.Ile1666Met) | dbSNP gnomAD v4 |
7 | g.128849377C>T | CA457849016 | FLNC | c.4998C>T (p.Ile1666=) | |
7 | g.128849378A>C | CA369203960 | FLNC | c.4999A>C (p.Thr1667Pro) | |
7 | g.128849378A>G | CA369203961 | FLNC | c.4999A>G (p.Thr1667Ala) | |
7 | g.128849378A>T | CA369203962 | FLNC | c.4999A>T (p.Thr1667Ser) | |
7 | g.128849379C>A | CA369203963 | FLNC | c.5000C>A (p.Thr1667Lys) | |
7 | g.128849379C= | CA1742564296 | FLNC | c.5000C= (p.Thr1667=) | |
7 | g.128849379C>G | CA369203964 | FLNC | c.5000C>G (p.Thr1667Arg) | ClinVar |
7 | g.128849379C>T | CA4475538 | FLNC | c.5000C>T (p.Thr1667Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849380G>A | CA4475539 | FLNC | c.5001G>A (p.Thr1667=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849380G>C | CA457849019 | FLNC | c.5001G>C (p.Thr1667=) | |
7 | g.128849380G= | CA1742564303 | FLNC | c.5001G= (p.Thr1667=) | |
7 | g.128849380G>T | CA457849020 | FLNC | c.5001G>T (p.Thr1667=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849381G>A | CA369203967 | FLNC | c.5002G>A (p.Val1668Met) | gnomAD v4 |
7 | g.128849381G>C | CA369203965 | FLNC | c.5002G>C (p.Val1668Leu) | |
7 | g.128849381G>T | CA369203966 | FLNC | c.5002G>T (p.Val1668Leu) | |
7 | g.128849382T>A | CA369203968 | FLNC | c.5003T>A (p.Val1668Glu) | |
7 | g.128849382T>C | CA369203969 | FLNC | c.5003T>C (p.Val1668Ala) | gnomAD v4 |
7 | g.128849382T>G | CA369203970 | FLNC | c.5003T>G (p.Val1668Gly) | |
7 | g.128849383G>A | CA4475540 | FLNC | c.5004G>A (p.Val1668=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.128849383G>C | CA457849028 | FLNC | c.5004G>C (p.Val1668=) | |
7 | g.128849383G= | CA1742564307 | FLNC | c.5004G= (p.Val1668=) | |
7 | g.128849383G>T | CA457849030 | FLNC | c.5004G>T (p.Val1668=) | |
7 | g.128849384G>A | CA369203971 | FLNC | c.5005G>A (p.Asp1669Asn) | |
7 | g.128849384G>C | CA369203972 | FLNC | c.5005G>C (p.Asp1669His) | |
7 | g.128849384G>T | CA369203973 | FLNC | c.5005G>T (p.Asp1669Tyr) | |
7 | g.128849385A>C | CA369203974 | FLNC | c.5006A>C (p.Asp1669Ala) | |
7 | g.128849385A>G | CA369203975 | FLNC | c.5006A>G (p.Asp1669Gly) | |
7 | g.128849385A>T | CA369203976 | FLNC | c.5006A>T (p.Asp1669Val) | |
7 | g.128849386T>A | CA369203978 | FLNC | c.5007T>A (p.Asp1669Glu) | |
7 | g.128849386T>C | CA4475541 | FLNC | c.5007T>C (p.Asp1669=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128849386T>G | CA369203977 | FLNC | c.5007T>G (p.Asp1669Glu) | |
7 | g.128849386T= | CA1742564316 | FLNC | c.5007T= (p.Asp1669=) | |
7 | g.128849387G>A | CA369203979 | FLNC | c.5008G>A (p.Ala1670Thr) | |
7 | g.128849387G>C | CA369203980 | FLNC | c.5008G>C (p.Ala1670Pro) | gnomAD v4 |
7 | g.128849387G>T | CA369203981 | FLNC | c.5008G>T (p.Ala1670Ser) | COSMIC |
7 | g.128849388C>A | CA369203982 | FLNC | c.5009C>A (p.Ala1670Asp) |