| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.178777179A= | CA1310617925 | TTN | c.4784T= (p.Ile1595=) c.4646T= (p.Ile1549=) n.254A= c.4832T= (p.Ile1611=) c.4691T= (p.Ile1564=) c.4829T= (p.Ile1610=) c.4787T= (p.Ile1596=) | |
| 2 | g.178777179A>C | CA60978210 | TTN | c.4784T>G (p.Ile1595Ser) c.4646T>G (p.Ile1549Ser) n.254A>C c.4832T>G (p.Ile1611Ser) c.4691T>G (p.Ile1564Ser) c.4829T>G (p.Ile1610Ser) c.4787T>G (p.Ile1596Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.178777179A>G | CA349461302 | TTN | c.4784T>C (p.Ile1595Thr) c.4646T>C (p.Ile1549Thr) n.254A>G c.4832T>C (p.Ile1611Thr) c.4691T>C (p.Ile1564Thr) c.4829T>C (p.Ile1610Thr) c.4787T>C (p.Ile1596Thr) | |
| 2 | g.178777179A>T | CA349461306 | TTN | c.4784T>A (p.Ile1595Asn) c.4646T>A (p.Ile1549Asn) n.254A>T c.4832T>A (p.Ile1611Asn) c.4691T>A (p.Ile1564Asn) c.4829T>A (p.Ile1610Asn) c.4787T>A (p.Ile1596Asn) | |
| 2 | g.178777180T>A | CA349461321 | TTN | c.4783A>T (p.Ile1595Phe) c.4645A>T (p.Ile1549Phe) n.255T>A c.4831A>T (p.Ile1611Phe) c.4690A>T (p.Ile1564Phe) c.4828A>T (p.Ile1610Phe) c.4786A>T (p.Ile1596Phe) | |
| 2 | g.178777180T>C | CA349461323 | TTN | c.4783A>G (p.Ile1595Val) c.4645A>G (p.Ile1549Val) n.255T>C c.4831A>G (p.Ile1611Val) c.4690A>G (p.Ile1564Val) c.4828A>G (p.Ile1610Val) c.4786A>G (p.Ile1596Val) | gnomAD v4 |
| 2 | g.178777180T>G | CA349461318 | TTN | c.4783A>C (p.Ile1595Leu) c.4645A>C (p.Ile1549Leu) n.255T>G c.4831A>C (p.Ile1611Leu) c.4690A>C (p.Ile1564Leu) c.4828A>C (p.Ile1610Leu) c.4786A>C (p.Ile1596Leu) | |
| 2 | g.178777181G>A | CA430281236 | TTN | c.4782C>T (p.Asp1594=) c.4644C>T (p.Asp1548=) n.256G>A c.4830C>T (p.Asp1610=) c.4689C>T (p.Asp1563=) c.4827C>T (p.Asp1609=) c.4785C>T (p.Asp1595=) | dbSNP gnomAD v4 |
| 2 | g.178777181G>C | CA349461341 | TTN | c.4782C>G (p.Asp1594Glu) c.4644C>G (p.Asp1548Glu) n.256G>C c.4830C>G (p.Asp1610Glu) c.4689C>G (p.Asp1563Glu) c.4827C>G (p.Asp1609Glu) c.4785C>G (p.Asp1595Glu) | |
| 2 | g.178777181G= | CA1310617926 | TTN | c.4782C= (p.Asp1594=) c.4644C= (p.Asp1548=) n.256G= c.4830C= (p.Asp1610=) c.4689C= (p.Asp1563=) c.4827C= (p.Asp1609=) c.4785C= (p.Asp1595=) | |
| 2 | g.178777181G>T | CA349461331 | TTN | c.4782C>A (p.Asp1594Glu) c.4644C>A (p.Asp1548Glu) n.256G>T c.4830C>A (p.Asp1610Glu) c.4689C>A (p.Asp1563Glu) c.4827C>A (p.Asp1609Glu) c.4785C>A (p.Asp1595Glu) | |
| 2 | g.178777182T>A | CA60978214 | TTN | c.4781A>T (p.Asp1594Val) c.4643A>T (p.Asp1548Val) n.257T>A c.4829A>T (p.Asp1610Val) c.4688A>T (p.Asp1563Val) c.4826A>T (p.Asp1609Val) c.4784A>T (p.Asp1595Val) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.178777182T>C | CA349461359 | TTN | c.4781A>G (p.Asp1594Gly) c.4643A>G (p.Asp1548Gly) n.257T>C c.4829A>G (p.Asp1610Gly) c.4688A>G (p.Asp1563Gly) c.4826A>G (p.Asp1609Gly) c.4784A>G (p.Asp1595Gly) | |
| 2 | g.178777182T>G | CA349461370 | TTN | c.4781A>C (p.Asp1594Ala) c.4643A>C (p.Asp1548Ala) n.257T>G c.4829A>C (p.Asp1610Ala) c.4688A>C (p.Asp1563Ala) c.4826A>C (p.Asp1609Ala) c.4784A>C (p.Asp1595Ala) | |
| 2 | g.178777182T= | CA1310617927 | TTN | c.4781A= (p.Asp1594=) c.4643A= (p.Asp1548=) n.257T= c.4829A= (p.Asp1610=) c.4688A= (p.Asp1563=) c.4826A= (p.Asp1609=) c.4784A= (p.Asp1595=) | |
| 2 | g.178777183C>A | CA349461378 | TTN | c.4780G>T (p.Asp1594Tyr) c.4642G>T (p.Asp1548Tyr) n.258C>A c.4828G>T (p.Asp1610Tyr) c.4687G>T (p.Asp1563Tyr) c.4825G>T (p.Asp1609Tyr) c.4783G>T (p.Asp1595Tyr) | |
| 2 | g.178777183C= | CA1310617928 | TTN | c.4780G= (p.Asp1594=) c.4642G= (p.Asp1548=) n.258C= c.4828G= (p.Asp1610=) c.4687G= (p.Asp1563=) c.4825G= (p.Asp1609=) c.4783G= (p.Asp1595=) | |
| 2 | g.178777183C>G | CA349461382 | TTN | c.4780G>C (p.Asp1594His) c.4642G>C (p.Asp1548His) n.258C>G c.4828G>C (p.Asp1610His) c.4687G>C (p.Asp1563His) c.4825G>C (p.Asp1609His) c.4783G>C (p.Asp1595His) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.178777183C>T | CA349461388 | TTN | c.4780G>A (p.Asp1594Asn) c.4642G>A (p.Asp1548Asn) n.258C>T c.4828G>A (p.Asp1610Asn) c.4687G>A (p.Asp1563Asn) c.4825G>A (p.Asp1609Asn) c.4783G>A (p.Asp1595Asn) | |
| 2 | g.178777184A>C | CA349461389 | TTN | c.4779T>G (p.Ser1593Arg) c.4641T>G (p.Ser1547Arg) n.259A>C c.4827T>G (p.Ser1609Arg) c.4686T>G (p.Ser1562Arg) c.4824T>G (p.Ser1608Arg) c.4782T>G (p.Ser1594Arg) | |
| 2 | g.178777184A>G | CA430281245 | TTN | c.4779T>C (p.Ser1593=) c.4641T>C (p.Ser1547=) n.259A>G c.4827T>C (p.Ser1609=) c.4686T>C (p.Ser1562=) c.4824T>C (p.Ser1608=) c.4782T>C (p.Ser1594=) | |
| 2 | g.178777184A>T | CA349461391 | TTN | c.4779T>A (p.Ser1593Arg) c.4641T>A (p.Ser1547Arg) n.259A>T c.4827T>A (p.Ser1609Arg) c.4686T>A (p.Ser1562Arg) c.4824T>A (p.Ser1608Arg) c.4782T>A (p.Ser1594Arg) | |
| 2 | g.178777185C>A | CA349461397 | TTN | c.4778G>T (p.Ser1593Ile) c.4640G>T (p.Ser1547Ile) n.260C>A c.4826G>T (p.Ser1609Ile) c.4685G>T (p.Ser1562Ile) c.4823G>T (p.Ser1608Ile) c.4781G>T (p.Ser1594Ile) | |
| 2 | g.178777185C>G | CA349461398 | TTN | c.4778G>C (p.Ser1593Thr) c.4640G>C (p.Ser1547Thr) n.260C>G c.4826G>C (p.Ser1609Thr) c.4685G>C (p.Ser1562Thr) c.4823G>C (p.Ser1608Thr) c.4781G>C (p.Ser1594Thr) | |
| 2 | g.178777185C>T | CA349461399 | TTN | c.4778G>A (p.Ser1593Asn) c.4640G>A (p.Ser1547Asn) n.260C>T c.4826G>A (p.Ser1609Asn) c.4685G>A (p.Ser1562Asn) c.4823G>A (p.Ser1608Asn) c.4781G>A (p.Ser1594Asn) | |
| 2 | g.178777186T>A | CA349461408 | TTN | c.4777A>T (p.Ser1593Cys) c.4639A>T (p.Ser1547Cys) n.261T>A c.4825A>T (p.Ser1609Cys) c.4684A>T (p.Ser1562Cys) c.4822A>T (p.Ser1608Cys) c.4780A>T (p.Ser1594Cys) | |
| 2 | g.178777186T>C | CA349461417 | TTN | c.4777A>G (p.Ser1593Gly) c.4639A>G (p.Ser1547Gly) n.261T>C c.4825A>G (p.Ser1609Gly) c.4684A>G (p.Ser1562Gly) c.4822A>G (p.Ser1608Gly) c.4780A>G (p.Ser1594Gly) | |
| 2 | g.178777186T>G | CA349461406 | TTN | c.4777A>C (p.Ser1593Arg) c.4639A>C (p.Ser1547Arg) n.261T>G c.4825A>C (p.Ser1609Arg) c.4684A>C (p.Ser1562Arg) c.4822A>C (p.Ser1608Arg) c.4780A>C (p.Ser1594Arg) | |
| 2 | g.178777187G>A | CA430281257 | TTN | c.4776C>T (p.Asn1592=) c.4638C>T (p.Asn1546=) n.262G>A c.4824C>T (p.Asn1608=) c.4683C>T (p.Asn1561=) c.4821C>T (p.Asn1607=) c.4779C>T (p.Asn1593=) | |
| 2 | g.178777187G>C | CA349461421 | TTN | c.4776C>G (p.Asn1592Lys) c.4638C>G (p.Asn1546Lys) n.262G>C c.4824C>G (p.Asn1608Lys) c.4683C>G (p.Asn1561Lys) c.4821C>G (p.Asn1607Lys) c.4779C>G (p.Asn1593Lys) | |
| 2 | g.178777187G>T | CA349461427 | TTN | c.4776C>A (p.Asn1592Lys) c.4638C>A (p.Asn1546Lys) n.262G>T c.4824C>A (p.Asn1608Lys) c.4683C>A (p.Asn1561Lys) c.4821C>A (p.Asn1607Lys) c.4779C>A (p.Asn1593Lys) | |
| 2 | g.178777188T>A | CA349461439 | TTN | c.4775A>T (p.Asn1592Ile) c.4637A>T (p.Asn1546Ile) n.263T>A c.4823A>T (p.Asn1608Ile) c.4682A>T (p.Asn1561Ile) c.4820A>T (p.Asn1607Ile) c.4778A>T (p.Asn1593Ile) | |
| 2 | g.178777188T>C | CA349461450 | TTN | c.4775A>G (p.Asn1592Ser) c.4637A>G (p.Asn1546Ser) n.263T>C c.4823A>G (p.Asn1608Ser) c.4682A>G (p.Asn1561Ser) c.4820A>G (p.Asn1607Ser) c.4778A>G (p.Asn1593Ser) | |
| 2 | g.178777188T>G | CA349461465 | TTN | c.4775A>C (p.Asn1592Thr) c.4637A>C (p.Asn1546Thr) n.263T>G c.4823A>C (p.Asn1608Thr) c.4682A>C (p.Asn1561Thr) c.4820A>C (p.Asn1607Thr) c.4778A>C (p.Asn1593Thr) | |
| 2 | g.178777189T>A | CA349461488 | TTN | c.4774A>T (p.Asn1592Tyr) c.4636A>T (p.Asn1546Tyr) n.264T>A c.4822A>T (p.Asn1608Tyr) c.4681A>T (p.Asn1561Tyr) c.4819A>T (p.Asn1607Tyr) c.4777A>T (p.Asn1593Tyr) | |
| 2 | g.178777189T>C | CA349461479 | TTN | c.4774A>G (p.Asn1592Asp) c.4636A>G (p.Asn1546Asp) n.264T>C c.4822A>G (p.Asn1608Asp) c.4681A>G (p.Asn1561Asp) c.4819A>G (p.Asn1607Asp) c.4777A>G (p.Asn1593Asp) | |
| 2 | g.178777189T>G | CA349461486 | TTN | c.4774A>C (p.Asn1592His) c.4636A>C (p.Asn1546His) n.264T>G c.4822A>C (p.Asn1608His) c.4681A>C (p.Asn1561His) c.4819A>C (p.Asn1607His) c.4777A>C (p.Asn1593His) | |
| 2 | g.178777190T>A | CA349461500 | TTN | c.4773A>T (p.Lys1591Asn) c.4635A>T (p.Lys1545Asn) n.265T>A c.4821A>T (p.Lys1607Asn) c.4680A>T (p.Lys1560Asn) c.4818A>T (p.Lys1606Asn) c.4776A>T (p.Lys1592Asn) | |
| 2 | g.178777190T>C | CA430281266 | TTN | c.4773A>G (p.Lys1591=) c.4635A>G (p.Lys1545=) n.265T>C c.4821A>G (p.Lys1607=) c.4680A>G (p.Lys1560=) c.4818A>G (p.Lys1606=) c.4776A>G (p.Lys1592=) | ClinVar |
| 2 | g.178777190T>G | CA349461501 | TTN | c.4773A>C (p.Lys1591Asn) c.4635A>C (p.Lys1545Asn) n.265T>G c.4821A>C (p.Lys1607Asn) c.4680A>C (p.Lys1560Asn) c.4818A>C (p.Lys1606Asn) c.4776A>C (p.Lys1592Asn) | |
| 2 | g.178777191T>A | CA349461504 | TTN | c.4772A>T (p.Lys1591Ile) c.4634A>T (p.Lys1545Ile) n.266T>A c.4820A>T (p.Lys1607Ile) c.4679A>T (p.Lys1560Ile) c.4817A>T (p.Lys1606Ile) c.4775A>T (p.Lys1592Ile) | |
| 2 | g.178777191T>C | CA349461508 | TTN | c.4772A>G (p.Lys1591Arg) c.4634A>G (p.Lys1545Arg) n.266T>C c.4820A>G (p.Lys1607Arg) c.4679A>G (p.Lys1560Arg) c.4817A>G (p.Lys1606Arg) c.4775A>G (p.Lys1592Arg) | dbSNP gnomAD v4 |
| 2 | g.178777191T>G | CA349461509 | TTN | c.4772A>C (p.Lys1591Thr) c.4634A>C (p.Lys1545Thr) n.266T>G c.4820A>C (p.Lys1607Thr) c.4679A>C (p.Lys1560Thr) c.4817A>C (p.Lys1606Thr) c.4775A>C (p.Lys1592Thr) | |
| 2 | g.178777191T= | CA1310617929 | TTN | c.4772A= (p.Lys1591=) c.4634A= (p.Lys1545=) n.266T= c.4820A= (p.Lys1607=) c.4679A= (p.Lys1560=) c.4817A= (p.Lys1606=) c.4775A= (p.Lys1592=) | |
| 2 | g.178777192T>A | CA349461518 | TTN | c.4771A>T (p.Lys1591Ter) c.4633A>T (p.Lys1545Ter) n.267T>A c.4819A>T (p.Lys1607Ter) c.4678A>T (p.Lys1560Ter) c.4816A>T (p.Lys1606Ter) c.4774A>T (p.Lys1592Ter) | |
| 2 | g.178777192T>C | CA349461516 | TTN | c.4771A>G (p.Lys1591Glu) c.4633A>G (p.Lys1545Glu) n.267T>C c.4819A>G (p.Lys1607Glu) c.4678A>G (p.Lys1560Glu) c.4816A>G (p.Lys1606Glu) c.4774A>G (p.Lys1592Glu) | |
| 2 | g.178777192T>G | CA349461515 | TTN | c.4771A>C (p.Lys1591Gln) c.4633A>C (p.Lys1545Gln) n.267T>G c.4819A>C (p.Lys1607Gln) c.4678A>C (p.Lys1560Gln) c.4816A>C (p.Lys1606Gln) c.4774A>C (p.Lys1592Gln) | |
| 2 | g.178777193C>A | CA349461520 | TTN | c.4770G>T (p.Leu1590Phe) c.4632G>T (p.Leu1544Phe) n.268C>A c.4818G>T (p.Leu1606Phe) c.4677G>T (p.Leu1559Phe) c.4815G>T (p.Leu1605Phe) c.4773G>T (p.Leu1591Phe) | |
| 2 | g.178777193C>G | CA349461528 | TTN | c.4770G>C (p.Leu1590Phe) c.4632G>C (p.Leu1544Phe) n.268C>G c.4818G>C (p.Leu1606Phe) c.4677G>C (p.Leu1559Phe) c.4815G>C (p.Leu1605Phe) c.4773G>C (p.Leu1591Phe) | ClinVar gnomAD v4 |
| 2 | g.178777193C>T | CA430281278 | TTN | c.4770G>A (p.Leu1590=) c.4632G>A (p.Leu1544=) n.268C>T c.4818G>A (p.Leu1606=) c.4677G>A (p.Leu1559=) c.4815G>A (p.Leu1605=) c.4773G>A (p.Leu1591=) |