Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128851563A= | CA1742571445 | FLNC,FLNC-AS1 | c.5777A= (p.Tyr1926=) c.5678A= (p.Tyr1893=) n.216-63T= | |
7 | g.128851563A>C | CA369208404 | FLNC,FLNC-AS1 | c.5777A>C (p.Tyr1926Ser) c.5678A>C (p.Tyr1893Ser) n.216-63T>G | |
7 | g.128851563A>G | CA4475780 | FLNC,FLNC-AS1 | c.5777A>G (p.Tyr1926Cys) c.5678A>G (p.Tyr1893Cys) n.216-63T>C | ClinVar dbSNP ExAC gnomAD v2 COSMIC |
7 | g.128851563A>T | CA369208406 | FLNC,FLNC-AS1 | c.5777A>T (p.Tyr1926Phe) c.5678A>T (p.Tyr1893Phe) n.216-63T>A | |
7 | g.128851564C>A | CA369208409 | FLNC,FLNC-AS1 | c.5778C>A (p.Tyr1926Ter) c.5679C>A (p.Tyr1893Ter) n.216-64G>T | |
7 | g.128851564C= | CA1742571473 | FLNC,FLNC-AS1 | c.5778C= (p.Tyr1926=) c.5679C= (p.Tyr1893=) n.216-64G= | |
7 | g.128851564C>G | CA369208411 | FLNC,FLNC-AS1 | c.5778C>G (p.Tyr1926Ter) c.5679C>G (p.Tyr1893Ter) n.216-64G>C | ClinVar |
7 | g.128851564C>T | CA4475781 | FLNC,FLNC-AS1 | c.5778C>T (p.Tyr1926=) c.5679C>T (p.Tyr1893=) n.216-64G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128851565A= | CA1742571476 | FLNC,FLNC-AS1 | c.5779A= (p.Ser1927=) c.5680A= (p.Ser1894=) n.216-65T= | |
7 | g.128851565A>C | CA369208415 | FLNC,FLNC-AS1 | c.5779A>C (p.Ser1927Arg) c.5680A>C (p.Ser1894Arg) n.216-65T>G | |
7 | g.128851565A>G | CA166189044 | FLNC,FLNC-AS1 | c.5779A>G (p.Ser1927Gly) c.5680A>G (p.Ser1894Gly) n.216-65T>C | ClinVar dbSNP |
7 | g.128851565A>T | CA369208414 | FLNC,FLNC-AS1 | c.5779A>T (p.Ser1927Cys) c.5680A>T (p.Ser1894Cys) n.216-65T>A | |
7 | g.128851566G>A | CA369208418 | FLNC,FLNC-AS1 | c.5780G>A (p.Ser1927Asn) c.5681G>A (p.Ser1894Asn) n.216-66C>T | dbSNP |
7 | g.128851566G>C | CA369208419 | FLNC,FLNC-AS1 | c.5780G>C (p.Ser1927Thr) c.5681G>C (p.Ser1894Thr) n.216-66C>G | |
7 | g.128851566G>T | CA369208421 | FLNC,FLNC-AS1 | c.5780G>T (p.Ser1927Ile) c.5681G>T (p.Ser1894Ile) n.216-66C>A | |
7 | g.128851567C>A | CA369208423 | FLNC,FLNC-AS1 | c.5781C>A (p.Ser1927Arg) c.5682C>A (p.Ser1894Arg) n.216-67G>T | |
7 | g.128851567C>G | CA369208425 | FLNC,FLNC-AS1 | c.5781C>G (p.Ser1927Arg) c.5682C>G (p.Ser1894Arg) n.216-67G>C | |
7 | g.128851567C>T | CA457849232 | FLNC,FLNC-AS1 | c.5781C>T (p.Ser1927=) c.5682C>T (p.Ser1894=) n.216-67G>A | |
7 | g.128851568A= | CA1742571484 | FLNC,FLNC-AS1 | c.5782A= (p.Ile1928=) c.5683A= (p.Ile1895=) n.216-68T= | |
7 | g.128851568A>C | CA369208426 | FLNC,FLNC-AS1 | c.5782A>C (p.Ile1928Leu) c.5683A>C (p.Ile1895Leu) n.216-68T>G | |
7 | g.128851568A>G | CA369208428 | FLNC,FLNC-AS1 | c.5782A>G (p.Ile1928Val) c.5683A>G (p.Ile1895Val) n.216-68T>C | dbSNP |
7 | g.128851568A>T | CA369208430 | FLNC,FLNC-AS1 | c.5782A>T (p.Ile1928Phe) c.5683A>T (p.Ile1895Phe) n.216-68T>A | |
7 | g.128851569T>A | CA369208432 | FLNC,FLNC-AS1 | c.5783T>A (p.Ile1928Asn) c.5684T>A (p.Ile1895Asn) n.216-69A>T | |
7 | g.128851569T>C | CA369208436 | FLNC,FLNC-AS1 | c.5783T>C (p.Ile1928Thr) c.5684T>C (p.Ile1895Thr) n.216-69A>G | |
7 | g.128851569T>G | CA369208434 | FLNC,FLNC-AS1 | c.5783T>G (p.Ile1928Ser) c.5684T>G (p.Ile1895Ser) n.216-69A>C | |
7 | g.128851570C>A | CA457849235 | FLNC,FLNC-AS1 | c.5784C>A (p.Ile1928=) c.5685C>A (p.Ile1895=) n.216-70G>T | |
7 | g.128851570C>G | CA369208438 | FLNC,FLNC-AS1 | c.5784C>G (p.Ile1928Met) c.5685C>G (p.Ile1895Met) n.216-70G>C | |
7 | g.128851570C>T | CA457849236 | FLNC,FLNC-AS1 | c.5784C>T (p.Ile1928=) c.5685C>T (p.Ile1895=) n.216-70G>A | gnomAD v4 |
7 | g.128851571A= | CA1742571488 | FLNC,FLNC-AS1 | c.5785A= (p.Ile1929=) c.5686A= (p.Ile1896=) n.216-71T= | |
7 | g.128851571A>C | CA369208440 | FLNC,FLNC-AS1 | c.5785A>C (p.Ile1929Leu) c.5686A>C (p.Ile1896Leu) n.216-71T>G | dbSNP |
7 | g.128851571A>G | CA369208442 | FLNC,FLNC-AS1 | c.5785A>G (p.Ile1929Val) c.5686A>G (p.Ile1896Val) n.216-71T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128851571A>T | CA369208445 | FLNC,FLNC-AS1 | c.5785A>T (p.Ile1929Phe) c.5686A>T (p.Ile1896Phe) n.216-71T>A | |
7 | g.128851572T>A | CA369208448 | FLNC,FLNC-AS1 | c.5786T>A (p.Ile1929Asn) c.5687T>A (p.Ile1896Asn) n.216-72A>T | |
7 | g.128851572T>C | CA369208451 | FLNC,FLNC-AS1 | c.5786T>C (p.Ile1929Thr) c.5687T>C (p.Ile1896Thr) n.216-72A>G | |
7 | g.128851572T>G | CA369208449 | FLNC,FLNC-AS1 | c.5786T>G (p.Ile1929Ser) c.5687T>G (p.Ile1896Ser) n.216-72A>C | |
7 | g.128851573C>A | CA457849240 | FLNC,FLNC-AS1 | c.5787C>A (p.Ile1929=) c.5688C>A (p.Ile1896=) n.216-73G>T | |
7 | g.128851573C= | CA1742571515 | FLNC,FLNC-AS1 | c.5787C= (p.Ile1929=) c.5688C= (p.Ile1896=) n.216-73G= | |
7 | g.128851573C>G | CA369208453 | FLNC,FLNC-AS1 | c.5787C>G (p.Ile1929Met) c.5688C>G (p.Ile1896Met) n.216-73G>C | |
7 | g.128851573C>T | CA4475782 | FLNC,FLNC-AS1 | c.5787C>T (p.Ile1929=) c.5688C>T (p.Ile1896=) n.216-73G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128851574G>A | CA4475783 | FLNC,FLNC-AS1 | c.5788G>A (p.Val1930Met) c.5689G>A (p.Val1897Met) n.216-74C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128851574G>C | CA369208456 | FLNC,FLNC-AS1 | c.5788G>C (p.Val1930Leu) c.5689G>C (p.Val1897Leu) n.216-74C>G | |
7 | g.128851574G= | CA1742571519 | FLNC,FLNC-AS1 | c.5788G= (p.Val1930=) c.5689G= (p.Val1897=) n.216-74C= | |
7 | g.128851574G>T | CA369208457 | FLNC,FLNC-AS1 | c.5788G>T (p.Val1930Leu) c.5689G>T (p.Val1897Leu) n.216-74C>A | |
7 | g.128851575_128851576del | CA2580076617 | FLNC,FLNC-AS1 | c.5789_5790del (p.Val1930AlafsTer4) c.5690_5691del (p.Val1897AlafsTer4) n.216-75_216-74del | ClinVar |
7 | g.128851575T>A | CA369208458 | FLNC,FLNC-AS1 | c.5789T>A (p.Val1930Glu) c.5690T>A (p.Val1897Glu) n.216-75A>T | |
7 | g.128851575T>C | CA369208459 | FLNC,FLNC-AS1 | c.5789T>C (p.Val1930Ala) c.5690T>C (p.Val1897Ala) n.216-75A>G | |
7 | g.128851575T>G | CA369208460 | FLNC,FLNC-AS1 | c.5789T>G (p.Val1930Gly) c.5690T>G (p.Val1897Gly) n.216-75A>C | |
7 | g.128851576G>A | CA4475784 | FLNC,FLNC-AS1 | c.5790G>A (p.Val1930=) c.5691G>A (p.Val1897=) n.216-76C>T | dbSNP ExAC gnomAD v2 |
7 | g.128851576G>C | CA457849242 | FLNC,FLNC-AS1 | c.5790G>C (p.Val1930=) c.5691G>C (p.Val1897=) n.216-76C>G | |
7 | g.128851576G= | CA1742571529 | FLNC,FLNC-AS1 | c.5790G= (p.Val1930=) c.5691G= (p.Val1897=) n.216-76C= |