Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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=) | |
7 | g.128849480A>C | CA369204180 | FLNC | c.5101A>C (p.Thr1701Pro) | |
7 | g.128849480A>G | CA369204181 | FLNC | c.5101A>G (p.Thr1701Ala) | |
7 | g.128849480A>T | CA369204182 | FLNC | c.5101A>T (p.Thr1701Ser) | |
7 | g.128849481C>A | CA369204183 | FLNC | c.5102C>A (p.Thr1701Asn) | |
7 | g.128849481C>G | CA369204184 | FLNC | c.5102C>G (p.Thr1701Ser) | |
7 | g.128849481C>T | CA369204185 | FLNC | c.5102C>T (p.Thr1701Ile) | |
7 | g.128849482C>A | CA457848961 | FLNC | c.5103C>A (p.Thr1701=) | |
7 | g.128849482C>G | CA457848962 | FLNC | c.5103C>G (p.Thr1701=) | |
7 | g.128849482C>T | CA457848963 | FLNC | c.5103C>T (p.Thr1701=) | gnomAD v4 |
7 | g.128849483T>A | CA369204186 | FLNC | c.5104T>A (p.Phe1702Ile) | |
7 | g.128849483T>C | CA369204187 | FLNC | c.5104T>C (p.Phe1702Leu) | |
7 | g.128849483T>G | CA369204188 | FLNC | c.5104T>G (p.Phe1702Val) | |
7 | g.128849484T>A | CA369204191 | FLNC | c.5105T>A (p.Phe1702Tyr) | |
7 | g.128849484T>C | CA369204189 | FLNC | c.5105T>C (p.Phe1702Ser) | |
7 | g.128849484T>G | CA369204190 | FLNC | c.5105T>G (p.Phe1702Cys) | |
7 | g.128849485T>A | CA369204192 | FLNC | c.5106T>A (p.Phe1702Leu) | |
7 | g.128849485T>C | CA457848966 | FLNC | c.5106T>C (p.Phe1702=) | |
7 | g.128849485T>G | CA369204193 | FLNC | c.5106T>G (p.Phe1702Leu) | |
7 | g.128849486G>A | CA369204194 | FLNC | c.5107G>A (p.Asp1703Asn) | |
7 | g.128849486G>C | CA369204195 | FLNC | c.5107G>C (p.Asp1703His) | |
7 | g.128849486G>T | CA369204196 | FLNC | c.5107G>T (p.Asp1703Tyr) | |
7 | g.128849487A>C | CA369204197 | FLNC | c.5108A>C (p.Asp1703Ala) | |
7 | g.128849487A>G | CA369204198 | FLNC | c.5108A>G (p.Asp1703Gly) | |
7 | g.128849487A>T | CA369204199 | FLNC | c.5108A>T (p.Asp1703Val) | |
7 | g.128849488C>A | CA369204200 | FLNC | c.5109C>A (p.Asp1703Glu) | |
7 | g.128849488C= | CA1742564657 | FLNC | c.5109C= (p.Asp1703=) | |
7 | g.128849488C>G | CA369204201 | FLNC | c.5109C>G (p.Asp1703Glu) | |
7 | g.128849488C>T | CA4475556 | FLNC | c.5109C>T (p.Asp1703=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128849489A>C | CA369204204 | FLNC | c.5110A>C (p.Ile1704Leu) |