| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.178776979T>A | CA349459795 | TTN | c.4885A>T (p.Thr1629Ser) c.4747A>T (p.Thr1583Ser) n.54T>A c.4933A>T (p.Thr1645Ser) c.4792A>T (p.Thr1598Ser) c.4930A>T (p.Thr1644Ser) c.4888A>T (p.Thr1630Ser) | |
| 2 | g.178776979T>C | CA349459797 | TTN | c.4885A>G (p.Thr1629Ala) c.4747A>G (p.Thr1583Ala) n.54T>C c.4933A>G (p.Thr1645Ala) c.4792A>G (p.Thr1598Ala) c.4930A>G (p.Thr1644Ala) c.4888A>G (p.Thr1630Ala) | gnomAD v4 |
| 2 | g.178776979T>G | CA349459799 | TTN | c.4885A>C (p.Thr1629Pro) c.4747A>C (p.Thr1583Pro) n.54T>G c.4933A>C (p.Thr1645Pro) c.4792A>C (p.Thr1598Pro) c.4930A>C (p.Thr1644Pro) c.4888A>C (p.Thr1630Pro) | |
| 2 | g.178776980A>C | CA349459809 | TTN | c.4884T>G (p.Tyr1628Ter) c.4746T>G (p.Tyr1582Ter) n.55A>C c.4932T>G (p.Tyr1644Ter) c.4791T>G (p.Tyr1597Ter) c.4929T>G (p.Tyr1643Ter) c.4887T>G (p.Tyr1629Ter) | |
| 2 | g.178776980A>G | CA430280516 | TTN | c.4884T>C (p.Tyr1628=) c.4746T>C (p.Tyr1582=) n.55A>G c.4932T>C (p.Tyr1644=) c.4791T>C (p.Tyr1597=) c.4929T>C (p.Tyr1643=) c.4887T>C (p.Tyr1629=) | |
| 2 | g.178776980A>T | CA349459805 | TTN | c.4884T>A (p.Tyr1628Ter) c.4746T>A (p.Tyr1582Ter) n.55A>T c.4932T>A (p.Tyr1644Ter) c.4791T>A (p.Tyr1597Ter) c.4929T>A (p.Tyr1643Ter) c.4887T>A (p.Tyr1629Ter) | |
| 2 | g.178776981T>A | CA349459814 | TTN | c.4883A>T (p.Tyr1628Phe) c.4745A>T (p.Tyr1582Phe) n.56T>A c.4931A>T (p.Tyr1644Phe) c.4790A>T (p.Tyr1597Phe) c.4928A>T (p.Tyr1643Phe) c.4886A>T (p.Tyr1629Phe) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.178776981T>C | CA349459819 | TTN | c.4883A>G (p.Tyr1628Cys) c.4745A>G (p.Tyr1582Cys) n.56T>C c.4931A>G (p.Tyr1644Cys) c.4790A>G (p.Tyr1597Cys) c.4928A>G (p.Tyr1643Cys) c.4886A>G (p.Tyr1629Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.178776981T>G | CA349459821 | TTN | c.4883A>C (p.Tyr1628Ser) c.4745A>C (p.Tyr1582Ser) n.56T>G c.4931A>C (p.Tyr1644Ser) c.4790A>C (p.Tyr1597Ser) c.4928A>C (p.Tyr1643Ser) c.4886A>C (p.Tyr1629Ser) | |
| 2 | g.178776981T= | CA1310617856 | TTN | c.4883A= (p.Tyr1628=) c.4745A= (p.Tyr1582=) n.56T= c.4931A= (p.Tyr1644=) c.4790A= (p.Tyr1597=) c.4928A= (p.Tyr1643=) c.4886A= (p.Tyr1629=) | |
| 2 | g.178776982A>C | CA349459825 | TTN | c.4882T>G (p.Tyr1628Asp) c.4744T>G (p.Tyr1582Asp) n.57A>C c.4930T>G (p.Tyr1644Asp) c.4789T>G (p.Tyr1597Asp) c.4927T>G (p.Tyr1643Asp) c.4885T>G (p.Tyr1629Asp) | |
| 2 | g.178776982A>G | CA349459829 | TTN | c.4882T>C (p.Tyr1628His) c.4744T>C (p.Tyr1582His) n.57A>G c.4930T>C (p.Tyr1644His) c.4789T>C (p.Tyr1597His) c.4927T>C (p.Tyr1643His) c.4885T>C (p.Tyr1629His) | |
| 2 | g.178776982A>T | CA349459833 | TTN | c.4882T>A (p.Tyr1628Asn) c.4744T>A (p.Tyr1582Asn) n.57A>T c.4930T>A (p.Tyr1644Asn) c.4789T>A (p.Tyr1597Asn) c.4927T>A (p.Tyr1643Asn) c.4885T>A (p.Tyr1629Asn) | |
| 2 | g.178776983C>A | CA349459839 | TTN | c.4881G>T (p.Trp1627Cys) c.4743G>T (p.Trp1581Cys) n.58C>A c.4929G>T (p.Trp1643Cys) c.4788G>T (p.Trp1596Cys) c.4926G>T (p.Trp1642Cys) c.4884G>T (p.Trp1628Cys) | |
| 2 | g.178776983C>G | CA349459863 | TTN | c.4881G>C (p.Trp1627Cys) c.4743G>C (p.Trp1581Cys) n.58C>G c.4929G>C (p.Trp1643Cys) c.4788G>C (p.Trp1596Cys) c.4926G>C (p.Trp1642Cys) c.4884G>C (p.Trp1628Cys) | |
| 2 | g.178776983C>T | CA349459864 | TTN | c.4881G>A (p.Trp1627Ter) c.4743G>A (p.Trp1581Ter) n.58C>T c.4929G>A (p.Trp1643Ter) c.4788G>A (p.Trp1596Ter) c.4926G>A (p.Trp1642Ter) c.4884G>A (p.Trp1628Ter) | gnomAD v4 |
| 2 | g.178776984C>A | CA349459865 | TTN | c.4880G>T (p.Trp1627Leu) c.4742G>T (p.Trp1581Leu) n.59C>A c.4928G>T (p.Trp1643Leu) c.4787G>T (p.Trp1596Leu) c.4925G>T (p.Trp1642Leu) c.4883G>T (p.Trp1628Leu) | |
| 2 | g.178776984C= | CA1310617857 | TTN | c.4880G= (p.Trp1627=) c.4742G= (p.Trp1581=) n.59C= c.4928G= (p.Trp1643=) c.4787G= (p.Trp1596=) c.4925G= (p.Trp1642=) c.4883G= (p.Trp1628=) | |
| 2 | g.178776984C>G | CA349459868 | TTN | c.4880G>C (p.Trp1627Ser) c.4742G>C (p.Trp1581Ser) n.59C>G c.4928G>C (p.Trp1643Ser) c.4787G>C (p.Trp1596Ser) c.4925G>C (p.Trp1642Ser) c.4883G>C (p.Trp1628Ser) | gnomAD v4 |
| 2 | g.178776984C>T | CA2005250 | TTN | c.4880G>A (p.Trp1627Ter) c.4742G>A (p.Trp1581Ter) n.59C>T c.4928G>A (p.Trp1643Ter) c.4787G>A (p.Trp1596Ter) c.4925G>A (p.Trp1642Ter) c.4883G>A (p.Trp1628Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.178776985A>C | CA349459871 | TTN | c.4879T>G (p.Trp1627Gly) c.4741T>G (p.Trp1581Gly) n.60A>C c.4927T>G (p.Trp1643Gly) c.4786T>G (p.Trp1596Gly) c.4924T>G (p.Trp1642Gly) c.4882T>G (p.Trp1628Gly) | |
| 2 | g.178776985A>G | CA349459877 | TTN | c.4879T>C (p.Trp1627Arg) c.4741T>C (p.Trp1581Arg) n.60A>G c.4927T>C (p.Trp1643Arg) c.4786T>C (p.Trp1596Arg) c.4924T>C (p.Trp1642Arg) c.4882T>C (p.Trp1628Arg) | |
| 2 | g.178776985A>T | CA349459872 | TTN | c.4879T>A (p.Trp1627Arg) c.4741T>A (p.Trp1581Arg) n.60A>T c.4927T>A (p.Trp1643Arg) c.4786T>A (p.Trp1596Arg) c.4924T>A (p.Trp1642Arg) c.4882T>A (p.Trp1628Arg) | gnomAD v4 |
| 2 | g.178776986G>A | CA430280524 | TTN | c.4878C>T (p.Ala1626=) c.4740C>T (p.Ala1580=) n.61G>A c.4926C>T (p.Ala1642=) c.4785C>T (p.Ala1595=) c.4923C>T (p.Ala1641=) c.4881C>T (p.Ala1627=) | gnomAD v4 |
| 2 | g.178776986G>C | CA430280526 | TTN | c.4878C>G (p.Ala1626=) c.4740C>G (p.Ala1580=) n.61G>C c.4926C>G (p.Ala1642=) c.4785C>G (p.Ala1595=) c.4923C>G (p.Ala1641=) c.4881C>G (p.Ala1627=) | |
| 2 | g.178776986G>T | CA430280528 | TTN | c.4878C>A (p.Ala1626=) c.4740C>A (p.Ala1580=) n.61G>T c.4926C>A (p.Ala1642=) c.4785C>A (p.Ala1595=) c.4923C>A (p.Ala1641=) c.4881C>A (p.Ala1627=) | |
| 2 | g.178776987G>A | CA349459884 | TTN | c.4877C>T (p.Ala1626Val) c.4739C>T (p.Ala1580Val) n.62G>A c.4925C>T (p.Ala1642Val) c.4784C>T (p.Ala1595Val) c.4922C>T (p.Ala1641Val) c.4880C>T (p.Ala1627Val) | gnomAD v4 |
| 2 | g.178776987G>C | CA349459893 | TTN | c.4877C>G (p.Ala1626Gly) c.4739C>G (p.Ala1580Gly) n.62G>C c.4925C>G (p.Ala1642Gly) c.4784C>G (p.Ala1595Gly) c.4922C>G (p.Ala1641Gly) c.4880C>G (p.Ala1627Gly) | |
| 2 | g.178776987G>T | CA349459888 | TTN | c.4877C>A (p.Ala1626Asp) c.4739C>A (p.Ala1580Asp) n.62G>T c.4925C>A (p.Ala1642Asp) c.4784C>A (p.Ala1595Asp) c.4922C>A (p.Ala1641Asp) c.4880C>A (p.Ala1627Asp) | |
| 2 | g.178776988C>A | CA349459897 | TTN | c.4876G>T (p.Ala1626Ser) c.4738G>T (p.Ala1580Ser) n.63C>A c.4924G>T (p.Ala1642Ser) c.4783G>T (p.Ala1595Ser) c.4921G>T (p.Ala1641Ser) c.4879G>T (p.Ala1627Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.178776988C= | CA1310617858 | TTN | c.4876G= (p.Ala1626=) c.4738G= (p.Ala1580=) n.63C= c.4924G= (p.Ala1642=) c.4783G= (p.Ala1595=) c.4921G= (p.Ala1641=) c.4879G= (p.Ala1627=) | |
| 2 | g.178776988C>G | CA349459899 | TTN | c.4876G>C (p.Ala1626Pro) c.4738G>C (p.Ala1580Pro) n.63C>G c.4924G>C (p.Ala1642Pro) c.4783G>C (p.Ala1595Pro) c.4921G>C (p.Ala1641Pro) c.4879G>C (p.Ala1627Pro) | |
| 2 | g.178776988C>T | CA349459901 | TTN | c.4876G>A (p.Ala1626Thr) c.4738G>A (p.Ala1580Thr) n.63C>T c.4924G>A (p.Ala1642Thr) c.4783G>A (p.Ala1595Thr) c.4921G>A (p.Ala1641Thr) c.4879G>A (p.Ala1627Thr) | dbSNP |
| 2 | g.178776989A>C | CA430280533 | TTN | c.4875T>G (p.Ser1625=) c.4737T>G (p.Ser1579=) n.64A>C c.4923T>G (p.Ser1641=) c.4782T>G (p.Ser1594=) c.4920T>G (p.Ser1640=) c.4878T>G (p.Ser1626=) | |
| 2 | g.178776989A>G | CA430280536 | TTN | c.4875T>C (p.Ser1625=) c.4737T>C (p.Ser1579=) n.64A>G c.4923T>C (p.Ser1641=) c.4782T>C (p.Ser1594=) c.4920T>C (p.Ser1640=) c.4878T>C (p.Ser1626=) | |
| 2 | g.178776989A>T | CA430280535 | TTN | c.4875T>A (p.Ser1625=) c.4737T>A (p.Ser1579=) n.64A>T c.4923T>A (p.Ser1641=) c.4782T>A (p.Ser1594=) c.4920T>A (p.Ser1640=) c.4878T>A (p.Ser1626=) | |
| 2 | g.178776990G>A | CA349459905 | TTN | c.4874C>T (p.Ser1625Phe) c.4736C>T (p.Ser1579Phe) n.65G>A c.4922C>T (p.Ser1641Phe) c.4781C>T (p.Ser1594Phe) c.4919C>T (p.Ser1640Phe) c.4877C>T (p.Ser1626Phe) | |
| 2 | g.178776990G>C | CA183649 | TTN | c.4874C>G (p.Ser1625Cys) c.4736C>G (p.Ser1579Cys) n.65G>C c.4922C>G (p.Ser1641Cys) c.4781C>G (p.Ser1594Cys) c.4919C>G (p.Ser1640Cys) c.4877C>G (p.Ser1626Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.178776990G= | CA1310617859 | TTN | c.4874C= (p.Ser1625=) c.4736C= (p.Ser1579=) n.65G= c.4922C= (p.Ser1641=) c.4781C= (p.Ser1594=) c.4919C= (p.Ser1640=) c.4877C= (p.Ser1626=) | |
| 2 | g.178776990G>T | CA349459916 | TTN | c.4874C>A (p.Ser1625Tyr) c.4736C>A (p.Ser1579Tyr) n.65G>T c.4922C>A (p.Ser1641Tyr) c.4781C>A (p.Ser1594Tyr) c.4919C>A (p.Ser1640Tyr) c.4877C>A (p.Ser1626Tyr) | |
| 2 | g.178776991A>C | CA349459923 | TTN | c.4873T>G (p.Ser1625Ala) c.4735T>G (p.Ser1579Ala) n.66A>C c.4921T>G (p.Ser1641Ala) c.4780T>G (p.Ser1594Ala) c.4918T>G (p.Ser1640Ala) c.4876T>G (p.Ser1626Ala) | |
| 2 | g.178776991A>G | CA349459930 | TTN | c.4873T>C (p.Ser1625Pro) c.4735T>C (p.Ser1579Pro) n.66A>G c.4921T>C (p.Ser1641Pro) c.4780T>C (p.Ser1594Pro) c.4918T>C (p.Ser1640Pro) c.4876T>C (p.Ser1626Pro) | |
| 2 | g.178776991A>T | CA349459935 | TTN | c.4873T>A (p.Ser1625Thr) c.4735T>A (p.Ser1579Thr) n.66A>T c.4921T>A (p.Ser1641Thr) c.4780T>A (p.Ser1594Thr) c.4918T>A (p.Ser1640Thr) c.4876T>A (p.Ser1626Thr) | |
| 2 | g.178776992A>C | CA349459943 | TTN | c.4872T>G (p.Asp1624Glu) c.4734T>G (p.Asp1578Glu) n.67A>C c.4920T>G (p.Asp1640Glu) c.4779T>G (p.Asp1593Glu) c.4917T>G (p.Asp1639Glu) c.4875T>G (p.Asp1625Glu) | |
| 2 | g.178776992A>G | CA430280548 | TTN | c.4872T>C (p.Asp1624=) c.4734T>C (p.Asp1578=) n.67A>G c.4920T>C (p.Asp1640=) c.4779T>C (p.Asp1593=) c.4917T>C (p.Asp1639=) c.4875T>C (p.Asp1625=) | |
| 2 | g.178776992A>T | CA349459947 | TTN | c.4872T>A (p.Asp1624Glu) c.4734T>A (p.Asp1578Glu) n.67A>T c.4920T>A (p.Asp1640Glu) c.4779T>A (p.Asp1593Glu) c.4917T>A (p.Asp1639Glu) c.4875T>A (p.Asp1625Glu) | |
| 2 | g.178776993T>A | CA349459969 | TTN | c.4871A>T (p.Asp1624Val) c.4733A>T (p.Asp1578Val) n.68T>A c.4919A>T (p.Asp1640Val) c.4778A>T (p.Asp1593Val) c.4916A>T (p.Asp1639Val) c.4874A>T (p.Asp1625Val) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.178776993T>C | CA349459956 | TTN | c.4871A>G (p.Asp1624Gly) c.4733A>G (p.Asp1578Gly) n.68T>C c.4919A>G (p.Asp1640Gly) c.4778A>G (p.Asp1593Gly) c.4916A>G (p.Asp1639Gly) c.4874A>G (p.Asp1625Gly) | |
| 2 | g.178776993T>G | CA349459965 | TTN | c.4871A>C (p.Asp1624Ala) c.4733A>C (p.Asp1578Ala) n.68T>G c.4919A>C (p.Asp1640Ala) c.4778A>C (p.Asp1593Ala) c.4916A>C (p.Asp1639Ala) c.4874A>C (p.Asp1625Ala) | |
| 2 | g.178776993T= | CA1310617860 | TTN | c.4871A= (p.Asp1624=) c.4733A= (p.Asp1578=) n.68T= c.4919A= (p.Asp1640=) c.4778A= (p.Asp1593=) c.4916A= (p.Asp1639=) c.4874A= (p.Asp1625=) |