Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128849569C>A | CA369204400 | FLNC | c.5190C>A (p.Phe1730Leu) | |
7 | g.128849569C>G | CA369204401 | FLNC | c.5190C>G (p.Phe1730Leu) | |
7 | g.128849569C>T | CA457849131 | FLNC | c.5190C>T (p.Phe1730=) | |
7 | g.128849570C>A | CA369204403 | FLNC | c.5191C>A (p.His1731Asn) | |
7 | g.128849570C= | CA1742565007 | FLNC | c.5191C= (p.His1731=) | |
7 | g.128849570C>G | CA369204406 | FLNC | c.5191C>G (p.His1731Asp) | dbSNP gnomAD v4 |
7 | g.128849570C>T | CA369204404 | FLNC | c.5191C>T (p.His1731Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849571A>C | CA369204407 | FLNC | c.5192A>C (p.His1731Pro) | |
7 | g.128849571A>G | CA369204408 | FLNC | c.5192A>G (p.His1731Arg) | gnomAD v4 |
7 | g.128849571A>T | CA369204409 | FLNC | c.5192A>T (p.His1731Leu) | |
7 | g.128849572C>A | CA369204411 | FLNC | c.5193C>A (p.His1731Gln) | |
7 | g.128849572C= | CA1742565016 | FLNC | c.5193C= (p.His1731=) | |
7 | g.128849572C>G | CA369204412 | FLNC | c.5193C>G (p.His1731Gln) | |
7 | g.128849572C>T | CA4475577 | FLNC | c.5193C>T (p.His1731=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849573G>A | CA4475578 | FLNC | c.5194G>A (p.Val1732Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849573G>C | CA4475579 | FLNC | c.5194G>C (p.Val1732Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849573G= | CA1742565024 | FLNC | c.5194G= (p.Val1732=) | |
7 | g.128849573G>T | CA369204416 | FLNC | c.5194G>T (p.Val1732Leu) | |
7 | g.128849574T>A | CA369204418 | FLNC | c.5195T>A (p.Val1732Glu) | |
7 | g.128849574T>C | CA369204419 | FLNC | c.5195T>C (p.Val1732Ala) | |
7 | g.128849574T>G | CA369204420 | FLNC | c.5195T>G (p.Val1732Gly) | |
7 | g.128849575G>A | CA457849143 | FLNC | c.5196G>A (p.Val1732=) | |
7 | g.128849575G>C | CA457849141 | FLNC | c.5196G>C (p.Val1732=) | |
7 | g.128849575G>T | CA457849142 | FLNC | c.5196G>T (p.Val1732=) | |
7 | g.128849576C>A | CA369204423 | FLNC | c.5197C>A (p.Leu1733Met) | |
7 | g.128849576C= | CA1742565033 | FLNC | c.5197C= (p.Leu1733=) | |
7 | g.128849576C>G | CA369204422 | FLNC | c.5197C>G (p.Leu1733Val) | |
7 | g.128849576C>T | CA457849144 | FLNC | c.5197C>T (p.Leu1733=) | dbSNP gnomAD v2 |
7 | g.128849577T>A | CA369204425 | FLNC | c.5198T>A (p.Leu1733Gln) | |
7 | g.128849577T>C | CA369204427 | FLNC | c.5198T>C (p.Leu1733Pro) | |
7 | g.128849577T>G | CA369204429 | FLNC | c.5198T>G (p.Leu1733Arg) | |
7 | g.128849578G>A | CA457849147 | FLNC | c.5199G>A (p.Leu1733=) | |
7 | g.128849578G>C | CA457849150 | FLNC | c.5199G>C (p.Leu1733=) | |
7 | g.128849578G>T | CA457849152 | FLNC | c.5199G>T (p.Leu1733=) | |
7 | g.128849579G>A | CA369204430 | FLNC | c.5199+1G>A (n.5199+1G>A) | ClinVar |
7 | g.128849579G>C | CA369204431 | FLNC | c.5199+1G>C (n.5199+1G>C) | ClinVar dbSNP |
7 | g.128849579G= | CA1742565046 | FLNC | c.5199+1G= (n.5199+1G=) | |
7 | g.128849579G>T | CA369204432 | FLNC | c.5199+1G>T (n.5199+1G>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849580T>A | CA166185600 | FLNC | c.5199+2T>A (n.5199+2T>A) | dbSNP |
7 | g.128849580T>C | CA166185623 | FLNC | c.5199+2T>C (n.5199+2T>C) | dbSNP |
7 | g.128849580T>G | CA369204433 | FLNC | c.5199+2T>G (n.5199+2T>G) | |
7 | g.128849580T= | CA1742565068 | FLNC | c.5199+2T= (n.5199+2T=) | |
7 | g.128849581A>G | CA2684816501 | FLNC | c.5199+3A>G (n.5199+3A>G) | gnomAD v4 |
7 | g.128849584T>G | CA2740094845 | FLNC | c.5199+6T>G (n.5199+6T>G) | ClinVar |
7 | g.128849585T>G | CA833138496 | FLNC | c.5199+7T>G (n.5199+7T>G) | dbSNP gnomAD v4 |
7 | g.128849585T= | CA1742565075 | FLNC | c.5199+7T= (n.5199+7T=) | |
7 | g.128849586C= | CA1742565084 | FLNC | c.5199+8C= (n.5199+8C=) | |
7 | g.128849586C>G | CA2579014431 | FLNC | c.5199+8C>G (n.5199+8C>G) | |
7 | g.128849586C>T | CA4475580 | FLNC | c.5199+8C>T (n.5199+8C>T) | dbSNP ExAC gnomAD v2 |
7 | g.128849587T>C | CA2740094846 | FLNC | c.5199+9T>C (n.5199+9T>C) | ClinVar |