Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128849465G>A | CA369204142 | FLNC | c.5086G>A (p.Glu1696Lys) | |
7 | g.128849465G>C | CA369204144 | FLNC | c.5086G>C (p.Glu1696Gln) | COSMIC |
7 | g.128849465G>T | CA369204143 | FLNC | c.5086G>T (p.Glu1696Ter) | |
7 | g.128849466A>C | CA369204145 | FLNC | c.5087A>C (p.Glu1696Ala) | |
7 | g.128849466A>G | CA369204146 | FLNC | c.5087A>G (p.Glu1696Gly) | |
7 | g.128849466A>T | CA369204147 | FLNC | c.5087A>T (p.Glu1696Val) | |
7 | g.128849467G>A | CA457848936 | FLNC | c.5088G>A (p.Glu1696=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128849467G>C | CA369204148 | FLNC | c.5088G>C (p.Glu1696Asp) | ClinVar dbSNP |
7 | g.128849467G= | CA1742564623 | FLNC | c.5088G= (p.Glu1696=) | |
7 | g.128849467G>T | CA369204149 | FLNC | c.5088G>T (p.Glu1696Asp) | |
7 | g.128849468A>C | CA369204150 | FLNC | c.5089A>C (p.Asn1697His) | |
7 | g.128849468A>G | CA369204151 | FLNC | c.5089A>G (p.Asn1697Asp) | |
7 | g.128849468A>T | CA369204152 | FLNC | c.5089A>T (p.Asn1697Tyr) | |
7 | g.128849469A>C | CA369204153 | FLNC | c.5090A>C (p.Asn1697Thr) | |
7 | g.128849469A>G | CA369204154 | FLNC | c.5090A>G (p.Asn1697Ser) | |
7 | g.128849469A>T | CA369204155 | FLNC | c.5090A>T (p.Asn1697Ile) | |
7 | g.128849470C>A | CA369204156 | FLNC | c.5091C>A (p.Asn1697Lys) | |
7 | g.128849470C>G | CA369204157 | FLNC | c.5091C>G (p.Asn1697Lys) | |
7 | g.128849470C>T | CA457848942 | FLNC | c.5091C>T (p.Asn1697=) | |
7 | g.128849471C>A | CA369204160 | FLNC | c.5092C>A (p.His1698Asn) | |
7 | g.128849471C>G | CA369204159 | FLNC | c.5092C>G (p.His1698Asp) | gnomAD v4 |
7 | g.128849471C>T | CA369204158 | FLNC | c.5092C>T (p.His1698Tyr) | |
7 | g.128849472A>C | CA369204161 | FLNC | c.5093A>C (p.His1698Pro) | |
7 | g.128849472A>G | CA369204162 | FLNC | c.5093A>G (p.His1698Arg) | COSMIC |
7 | g.128849472A>T | CA369204163 | FLNC | c.5093A>T (p.His1698Leu) | |
7 | g.128849473T>A | CA369204164 | FLNC | c.5094T>A (p.His1698Gln) | |
7 | g.128849473T>C | CA457848948 | FLNC | c.5094T>C (p.His1698=) | dbSNP gnomAD v4 |
7 | g.128849473T>G | CA369204165 | FLNC | c.5094T>G (p.His1698Gln) | |
7 | g.128849473T= | CA1742564636 | FLNC | c.5094T= (p.His1698=) | |
7 | g.128849474G>A | CA369204166 | FLNC | c.5095G>A (p.Asp1699Asn) | |
7 | g.128849474G>C | CA369204167 | FLNC | c.5095G>C (p.Asp1699His) | |
7 | g.128849474G>T | CA369204168 | FLNC | c.5095G>T (p.Asp1699Tyr) | |
7 | g.128849475A>C | CA369204169 | FLNC | c.5096A>C (p.Asp1699Ala) | |
7 | g.128849475A>G | CA369204170 | FLNC | c.5096A>G (p.Asp1699Gly) | |
7 | g.128849475A>T | CA369204171 | FLNC | c.5096A>T (p.Asp1699Val) | |
7 | g.128849476C>A | CA369204172 | FLNC | c.5097C>A (p.Asp1699Glu) | |
7 | g.128849476C= | CA1742564639 | FLNC | c.5097C= (p.Asp1699=) | |
7 | g.128849476C>G | CA369204173 | FLNC | c.5097C>G (p.Asp1699Glu) | COSMIC |
7 | g.128849476C>T | CA457848952 | FLNC | c.5097C>T (p.Asp1699=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128849477G>A | CA369204175 | FLNC | c.5098G>A (p.Gly1700Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849477G>C | CA369204176 | FLNC | c.5098G>C (p.Gly1700Arg) | |
7 | g.128849477G= | CA1742564646 | FLNC | c.5098G= (p.Gly1700=) | |
7 | g.128849477G>T | CA369204174 | FLNC | c.5098G>T (p.Gly1700Cys) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128849478G>A | CA369204177 | FLNC | c.5099G>A (p.Gly1700Asp) | |
7 | g.128849478G>C | CA369204178 | FLNC | c.5099G>C (p.Gly1700Ala) | |
7 | g.128849478G>T | CA369204179 | FLNC | c.5099G>T (p.Gly1700Val) | |
7 | g.128849479T>A | CA457848957 | FLNC | c.5100T>A (p.Gly1700=) | |
7 | g.128849479T>C | CA457848955 | FLNC | c.5100T>C (p.Gly1700=) | gnomAD v4 |
7 | g.128849479T>G | CA457848954 | FLNC | c.5100T>G (p.Gly1700=) | dbSNP |
7 | g.128849479T= | CA1742564648 | FLNC | c.5100T= (p.Gly1700=) |