| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.33164855C>A | CA449867223 | COL11A2 | n.666G>T c.4860G>T (p.Thr1620=) c.4539G>T (p.Thr1513=) c.4602G>T (p.Thr1534=) n.650G>T c.4014G>T (p.Thr1338=) c.4146G>T (p.Thr1382=) c.3966G>T (p.Thr1322=) c.3903G>T (p.Thr1301=) c.3747G>T (p.Thr1249=) c.3678G>T (p.Thr1226=) | dbSNP gnomAD v4 |
| 6 | g.33164855C= | CA1619890404 | COL11A2 | n.666G= c.4860G= (p.Thr1620=) c.4539G= (p.Thr1513=) c.4602G= (p.Thr1534=) n.650G= c.4014G= (p.Thr1338=) c.4146G= (p.Thr1382=) c.3966G= (p.Thr1322=) c.3903G= (p.Thr1301=) c.3747G= (p.Thr1249=) c.3678G= (p.Thr1226=) | |
| 6 | g.33164855C>G | CA449867224 | COL11A2 | n.666G>C c.4860G>C (p.Thr1620=) c.4539G>C (p.Thr1513=) c.4602G>C (p.Thr1534=) n.650G>C c.4014G>C (p.Thr1338=) c.4146G>C (p.Thr1382=) c.3966G>C (p.Thr1322=) c.3903G>C (p.Thr1301=) c.3747G>C (p.Thr1249=) c.3678G>C (p.Thr1226=) | |
| 6 | g.33164855C>T | CA3749985 | COL11A2 | n.666G>A c.4860G>A (p.Thr1620=) c.4539G>A (p.Thr1513=) c.4602G>A (p.Thr1534=) n.650G>A c.4014G>A (p.Thr1338=) c.4146G>A (p.Thr1382=) c.3966G>A (p.Thr1322=) c.3903G>A (p.Thr1301=) c.3747G>A (p.Thr1249=) c.3678G>A (p.Thr1226=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.33164856G>A | CA3749986 | COL11A2 | n.665C>T c.4859C>T (p.Thr1620Met) c.4538C>T (p.Thr1513Met) c.4601C>T (p.Thr1534Met) n.649C>T c.4013C>T (p.Thr1338Met) c.4145C>T (p.Thr1382Met) c.3965C>T (p.Thr1322Met) c.3902C>T (p.Thr1301Met) c.3746C>T (p.Thr1249Met) c.3677C>T (p.Thr1226Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.33164856G>C | CA363617377 | COL11A2 | n.665C>G c.4859C>G (p.Thr1620Arg) c.4538C>G (p.Thr1513Arg) c.4601C>G (p.Thr1534Arg) n.649C>G c.4013C>G (p.Thr1338Arg) c.4145C>G (p.Thr1382Arg) c.3965C>G (p.Thr1322Arg) c.3902C>G (p.Thr1301Arg) c.3746C>G (p.Thr1249Arg) c.3677C>G (p.Thr1226Arg) | |
| 6 | g.33164856G= | CA1619890409 | COL11A2 | n.665C= c.4859C= (p.Thr1620=) c.4538C= (p.Thr1513=) c.4601C= (p.Thr1534=) n.649C= c.4013C= (p.Thr1338=) c.4145C= (p.Thr1382=) c.3965C= (p.Thr1322=) c.3902C= (p.Thr1301=) c.3746C= (p.Thr1249=) c.3677C= (p.Thr1226=) | |
| 6 | g.33164856G>T | CA363617380 | COL11A2 | n.665C>A c.4859C>A (p.Thr1620Lys) c.4538C>A (p.Thr1513Lys) c.4601C>A (p.Thr1534Lys) n.649C>A c.4013C>A (p.Thr1338Lys) c.4145C>A (p.Thr1382Lys) c.3965C>A (p.Thr1322Lys) c.3902C>A (p.Thr1301Lys) c.3746C>A (p.Thr1249Lys) c.3677C>A (p.Thr1226Lys) | dbSNP gnomAD v4 |
| 6 | g.33164857T>A | CA363617382 | COL11A2 | n.664A>T c.4858A>T (p.Thr1620Ser) c.4537A>T (p.Thr1513Ser) c.4600A>T (p.Thr1534Ser) n.648A>T c.4012A>T (p.Thr1338Ser) c.4144A>T (p.Thr1382Ser) c.3964A>T (p.Thr1322Ser) c.3901A>T (p.Thr1301Ser) c.3745A>T (p.Thr1249Ser) c.3676A>T (p.Thr1226Ser) | |
| 6 | g.33164857T>C | CA363617383 | COL11A2 | n.664A>G c.4858A>G (p.Thr1620Ala) c.4537A>G (p.Thr1513Ala) c.4600A>G (p.Thr1534Ala) n.648A>G c.4012A>G (p.Thr1338Ala) c.4144A>G (p.Thr1382Ala) c.3964A>G (p.Thr1322Ala) c.3901A>G (p.Thr1301Ala) c.3745A>G (p.Thr1249Ala) c.3676A>G (p.Thr1226Ala) | |
| 6 | g.33164857T>G | CA363617385 | COL11A2 | n.664A>C c.4858A>C (p.Thr1620Pro) c.4537A>C (p.Thr1513Pro) c.4600A>C (p.Thr1534Pro) n.648A>C c.4012A>C (p.Thr1338Pro) c.4144A>C (p.Thr1382Pro) c.3964A>C (p.Thr1322Pro) c.3901A>C (p.Thr1301Pro) c.3745A>C (p.Thr1249Pro) c.3676A>C (p.Thr1226Pro) | |
| 6 | g.33164858G>A | CA449867229 | COL11A2 | n.663C>T c.4857C>T (p.Val1619=) c.4536C>T (p.Val1512=) c.4599C>T (p.Val1533=) n.647C>T c.4011C>T (p.Val1337=) c.4143C>T (p.Val1381=) c.3963C>T (p.Val1321=) c.3900C>T (p.Val1300=) c.3744C>T (p.Val1248=) c.3675C>T (p.Val1225=) | |
| 6 | g.33164858G>C | CA449867231 | COL11A2 | n.663C>G c.4857C>G (p.Val1619=) c.4536C>G (p.Val1512=) c.4599C>G (p.Val1533=) n.647C>G c.4011C>G (p.Val1337=) c.4143C>G (p.Val1381=) c.3963C>G (p.Val1321=) c.3900C>G (p.Val1300=) c.3744C>G (p.Val1248=) c.3675C>G (p.Val1225=) | gnomAD v3 gnomAD v4 |
| 6 | g.33164858G>T | CA449867230 | COL11A2 | n.663C>A c.4857C>A (p.Val1619=) c.4536C>A (p.Val1512=) c.4599C>A (p.Val1533=) n.647C>A c.4011C>A (p.Val1337=) c.4143C>A (p.Val1381=) c.3963C>A (p.Val1321=) c.3900C>A (p.Val1300=) c.3744C>A (p.Val1248=) c.3675C>A (p.Val1225=) | |
| 6 | g.33164859A= | CA1619890415 | COL11A2 | n.662T= c.4856T= (p.Val1619=) c.4535T= (p.Val1512=) c.4598T= (p.Val1533=) n.646T= c.4010T= (p.Val1337=) c.4142T= (p.Val1381=) c.3962T= (p.Val1321=) c.3899T= (p.Val1300=) c.3743T= (p.Val1248=) c.3674T= (p.Val1225=) | |
| 6 | g.33164859A>C | CA363617391 | COL11A2 | n.662T>G c.4856T>G (p.Val1619Gly) c.4535T>G (p.Val1512Gly) c.4598T>G (p.Val1533Gly) n.646T>G c.4010T>G (p.Val1337Gly) c.4142T>G (p.Val1381Gly) c.3962T>G (p.Val1321Gly) c.3899T>G (p.Val1300Gly) c.3743T>G (p.Val1248Gly) c.3674T>G (p.Val1225Gly) | |
| 6 | g.33164859A>G | CA3749987 | COL11A2 | n.662T>C c.4856T>C (p.Val1619Ala) c.4535T>C (p.Val1512Ala) c.4598T>C (p.Val1533Ala) n.646T>C c.4010T>C (p.Val1337Ala) c.4142T>C (p.Val1381Ala) c.3962T>C (p.Val1321Ala) c.3899T>C (p.Val1300Ala) c.3743T>C (p.Val1248Ala) c.3674T>C (p.Val1225Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 6 | g.33164859A>T | CA363617387 | COL11A2 | n.662T>A c.4856T>A (p.Val1619Asp) c.4535T>A (p.Val1512Asp) c.4598T>A (p.Val1533Asp) n.646T>A c.4010T>A (p.Val1337Asp) c.4142T>A (p.Val1381Asp) c.3962T>A (p.Val1321Asp) c.3899T>A (p.Val1300Asp) c.3743T>A (p.Val1248Asp) c.3674T>A (p.Val1225Asp) | dbSNP gnomAD v2 |
| 6 | g.33164860C>A | CA363617394 | COL11A2 | n.661G>T c.4855G>T (p.Val1619Phe) c.4534G>T (p.Val1512Phe) c.4597G>T (p.Val1533Phe) n.645G>T c.4009G>T (p.Val1337Phe) c.4141G>T (p.Val1381Phe) c.3961G>T (p.Val1321Phe) c.3898G>T (p.Val1300Phe) c.3742G>T (p.Val1248Phe) c.3673G>T (p.Val1225Phe) | |
| 6 | g.33164860C= | CA1619890421 | COL11A2 | n.661G= c.4855G= (p.Val1619=) c.4534G= (p.Val1512=) c.4597G= (p.Val1533=) n.645G= c.4009G= (p.Val1337=) c.4141G= (p.Val1381=) c.3961G= (p.Val1321=) c.3898G= (p.Val1300=) c.3742G= (p.Val1248=) c.3673G= (p.Val1225=) | |
| 6 | g.33164860C>G | CA363617395 | COL11A2 | n.661G>C c.4855G>C (p.Val1619Leu) c.4534G>C (p.Val1512Leu) c.4597G>C (p.Val1533Leu) n.645G>C c.4009G>C (p.Val1337Leu) c.4141G>C (p.Val1381Leu) c.3961G>C (p.Val1321Leu) c.3898G>C (p.Val1300Leu) c.3742G>C (p.Val1248Leu) c.3673G>C (p.Val1225Leu) | |
| 6 | g.33164860C>T | CA363617396 | COL11A2 | n.661G>A c.4855G>A (p.Val1619Ile) c.4534G>A (p.Val1512Ile) c.4597G>A (p.Val1533Ile) n.645G>A c.4009G>A (p.Val1337Ile) c.4141G>A (p.Val1381Ile) c.3961G>A (p.Val1321Ile) c.3898G>A (p.Val1300Ile) c.3742G>A (p.Val1248Ile) c.3673G>A (p.Val1225Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.33164861G>A | CA3749988 | COL11A2 | n.660C>T c.4854C>T (p.Asp1618=) c.4533C>T (p.Asp1511=) c.4596C>T (p.Asp1532=) n.644C>T c.4008C>T (p.Asp1336=) c.4140C>T (p.Asp1380=) c.3960C>T (p.Asp1320=) c.3897C>T (p.Asp1299=) c.3741C>T (p.Asp1247=) c.3672C>T (p.Asp1224=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 6 | g.33164861G>C | CA3749989 | COL11A2 | n.660C>G c.4854C>G (p.Asp1618Glu) c.4533C>G (p.Asp1511Glu) c.4596C>G (p.Asp1532Glu) n.644C>G c.4008C>G (p.Asp1336Glu) c.4140C>G (p.Asp1380Glu) c.3960C>G (p.Asp1320Glu) c.3897C>G (p.Asp1299Glu) c.3741C>G (p.Asp1247Glu) c.3672C>G (p.Asp1224Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 6 | g.33164861G= | CA1619890425 | COL11A2 | n.660C= c.4854C= (p.Asp1618=) c.4533C= (p.Asp1511=) c.4596C= (p.Asp1532=) n.644C= c.4008C= (p.Asp1336=) c.4140C= (p.Asp1380=) c.3960C= (p.Asp1320=) c.3897C= (p.Asp1299=) c.3741C= (p.Asp1247=) c.3672C= (p.Asp1224=) | |
| 6 | g.33164861G>T | CA363617400 | COL11A2 | n.660C>A c.4854C>A (p.Asp1618Glu) c.4533C>A (p.Asp1511Glu) c.4596C>A (p.Asp1532Glu) n.644C>A c.4008C>A (p.Asp1336Glu) c.4140C>A (p.Asp1380Glu) c.3960C>A (p.Asp1320Glu) c.3897C>A (p.Asp1299Glu) c.3741C>A (p.Asp1247Glu) c.3672C>A (p.Asp1224Glu) | ClinVar |
| 6 | g.33164862T>A | CA363617401 | COL11A2 | n.659A>T c.4853A>T (p.Asp1618Val) c.4532A>T (p.Asp1511Val) c.4595A>T (p.Asp1532Val) n.643A>T c.4007A>T (p.Asp1336Val) c.4139A>T (p.Asp1380Val) c.3959A>T (p.Asp1320Val) c.3896A>T (p.Asp1299Val) c.3740A>T (p.Asp1247Val) c.3671A>T (p.Asp1224Val) | |
| 6 | g.33164862T>C | CA363617405 | COL11A2 | n.659A>G c.4853A>G (p.Asp1618Gly) c.4532A>G (p.Asp1511Gly) c.4595A>G (p.Asp1532Gly) n.643A>G c.4007A>G (p.Asp1336Gly) c.4139A>G (p.Asp1380Gly) c.3959A>G (p.Asp1320Gly) c.3896A>G (p.Asp1299Gly) c.3740A>G (p.Asp1247Gly) c.3671A>G (p.Asp1224Gly) | |
| 6 | g.33164862T>G | CA363617403 | COL11A2 | n.659A>C c.4853A>C (p.Asp1618Ala) c.4532A>C (p.Asp1511Ala) c.4595A>C (p.Asp1532Ala) n.643A>C c.4007A>C (p.Asp1336Ala) c.4139A>C (p.Asp1380Ala) c.3959A>C (p.Asp1320Ala) c.3896A>C (p.Asp1299Ala) c.3740A>C (p.Asp1247Ala) c.3671A>C (p.Asp1224Ala) | |
| 6 | g.33164863C>A | CA363617406 | COL11A2 | n.658G>T c.4852G>T (p.Asp1618Tyr) c.4531G>T (p.Asp1511Tyr) c.4594G>T (p.Asp1532Tyr) n.642G>T c.4006G>T (p.Asp1336Tyr) c.4138G>T (p.Asp1380Tyr) c.3958G>T (p.Asp1320Tyr) c.3895G>T (p.Asp1299Tyr) c.3739G>T (p.Asp1247Tyr) c.3670G>T (p.Asp1224Tyr) | gnomAD v4 |
| 6 | g.33164863C>G | CA363617408 | COL11A2 | n.658G>C c.4852G>C (p.Asp1618His) c.4531G>C (p.Asp1511His) c.4594G>C (p.Asp1532His) n.642G>C c.4006G>C (p.Asp1336His) c.4138G>C (p.Asp1380His) c.3958G>C (p.Asp1320His) c.3895G>C (p.Asp1299His) c.3739G>C (p.Asp1247His) c.3670G>C (p.Asp1224His) | |
| 6 | g.33164863C>T | CA363617410 | COL11A2 | n.658G>A c.4852G>A (p.Asp1618Asn) c.4531G>A (p.Asp1511Asn) c.4594G>A (p.Asp1532Asn) n.642G>A c.4006G>A (p.Asp1336Asn) c.4138G>A (p.Asp1380Asn) c.3958G>A (p.Asp1320Asn) c.3895G>A (p.Asp1299Asn) c.3739G>A (p.Asp1247Asn) c.3670G>A (p.Asp1224Asn) | |
| 6 | g.33164864A>C | CA363617412 | COL11A2 | n.657T>G c.4851T>G (p.Asp1617Glu) c.4530T>G (p.Asp1510Glu) c.4593T>G (p.Asp1531Glu) n.641T>G c.4005T>G (p.Asp1335Glu) c.4137T>G (p.Asp1379Glu) c.3957T>G (p.Asp1319Glu) c.3894T>G (p.Asp1298Glu) c.3738T>G (p.Asp1246Glu) c.3669T>G (p.Asp1223Glu) | |
| 6 | g.33164864A>G | CA449867243 | COL11A2 | n.657T>C c.4851T>C (p.Asp1617=) c.4530T>C (p.Asp1510=) c.4593T>C (p.Asp1531=) n.641T>C c.4005T>C (p.Asp1335=) c.4137T>C (p.Asp1379=) c.3957T>C (p.Asp1319=) c.3894T>C (p.Asp1298=) c.3738T>C (p.Asp1246=) c.3669T>C (p.Asp1223=) | |
| 6 | g.33164864A>T | CA363617413 | COL11A2 | n.657T>A c.4851T>A (p.Asp1617Glu) c.4530T>A (p.Asp1510Glu) c.4593T>A (p.Asp1531Glu) n.641T>A c.4005T>A (p.Asp1335Glu) c.4137T>A (p.Asp1379Glu) c.3957T>A (p.Asp1319Glu) c.3894T>A (p.Asp1298Glu) c.3738T>A (p.Asp1246Glu) c.3669T>A (p.Asp1223Glu) | |
| 6 | g.33164865T>A | CA363617417 | COL11A2 | n.656A>T c.4850A>T (p.Asp1617Val) c.4529A>T (p.Asp1510Val) c.4592A>T (p.Asp1531Val) n.640A>T c.4004A>T (p.Asp1335Val) c.4136A>T (p.Asp1379Val) c.3956A>T (p.Asp1319Val) c.3893A>T (p.Asp1298Val) c.3737A>T (p.Asp1246Val) c.3668A>T (p.Asp1223Val) | |
| 6 | g.33164865T>C | CA363617419 | COL11A2 | n.656A>G c.4850A>G (p.Asp1617Gly) c.4529A>G (p.Asp1510Gly) c.4592A>G (p.Asp1531Gly) n.640A>G c.4004A>G (p.Asp1335Gly) c.4136A>G (p.Asp1379Gly) c.3956A>G (p.Asp1319Gly) c.3893A>G (p.Asp1298Gly) c.3737A>G (p.Asp1246Gly) c.3668A>G (p.Asp1223Gly) | |
| 6 | g.33164865T>G | CA363617420 | COL11A2 | n.656A>C c.4850A>C (p.Asp1617Ala) c.4529A>C (p.Asp1510Ala) c.4592A>C (p.Asp1531Ala) n.640A>C c.4004A>C (p.Asp1335Ala) c.4136A>C (p.Asp1379Ala) c.3956A>C (p.Asp1319Ala) c.3893A>C (p.Asp1298Ala) c.3737A>C (p.Asp1246Ala) c.3668A>C (p.Asp1223Ala) | |
| 6 | g.33164865_33164866delinsTC | CA1619890432 | COL11A2 | n.655_656delinsGA c.4849_4850delinsGA (p.Asp1617=) c.4528_4529delinsGA (p.Asp1510=) c.4591_4592delinsGA (p.Asp1531=) n.639_640delinsGA c.4003_4004delinsGA (p.Asp1335=) c.4135_4136delinsGA (p.Asp1379=) c.3955_3956delinsGA (p.Asp1319=) c.3892_3893delinsGA (p.Asp1298=) c.3736_3737delinsGA (p.Asp1246=) c.3667_3668delinsGA (p.Asp1223=) | |
| 6 | g.33164866C>A | CA363617422 | COL11A2 | n.655G>T c.4849G>T (p.Asp1617Tyr) c.4528G>T (p.Asp1510Tyr) c.4591G>T (p.Asp1531Tyr) n.639G>T c.4003G>T (p.Asp1335Tyr) c.4135G>T (p.Asp1379Tyr) c.3955G>T (p.Asp1319Tyr) c.3892G>T (p.Asp1298Tyr) c.3736G>T (p.Asp1246Tyr) c.3667G>T (p.Asp1223Tyr) | dbSNP gnomAD v4 |
| 6 | g.33164866C= | CA1619890436 | COL11A2 | n.655G= c.4849G= (p.Asp1617=) c.4528G= (p.Asp1510=) c.4591G= (p.Asp1531=) n.639G= c.4003G= (p.Asp1335=) c.4135G= (p.Asp1379=) c.3955G= (p.Asp1319=) c.3892G= (p.Asp1298=) c.3736G= (p.Asp1246=) c.3667G= (p.Asp1223=) | |
| 6 | g.33164866C>G | CA363617424 | COL11A2 | n.655G>C c.4849G>C (p.Asp1617His) c.4528G>C (p.Asp1510His) c.4591G>C (p.Asp1531His) n.639G>C c.4003G>C (p.Asp1335His) c.4135G>C (p.Asp1379His) c.3955G>C (p.Asp1319His) c.3892G>C (p.Asp1298His) c.3736G>C (p.Asp1246His) c.3667G>C (p.Asp1223His) | |
| 6 | g.33164866C>T | CA363617426 | COL11A2 | n.655G>A c.4849G>A (p.Asp1617Asn) c.4528G>A (p.Asp1510Asn) c.4591G>A (p.Asp1531Asn) n.639G>A c.4003G>A (p.Asp1335Asn) c.4135G>A (p.Asp1379Asn) c.3955G>A (p.Asp1319Asn) c.3892G>A (p.Asp1298Asn) c.3736G>A (p.Asp1246Asn) c.3667G>A (p.Asp1223Asn) | |
| 6 | g.33164868del | CA566424989 | COL11A2 | n.655del c.4849del (p.Asp1617MetfsTer?) c.4528del (p.Asp1510MetfsTer?) c.4591del (p.Asp1531MetfsTer?) n.639del c.4003del (p.Asp1335MetfsTer?) c.4135del (p.Asp1379MetfsTer?) c.3955del (p.Asp1319MetfsTer?) c.3892del (p.Asp1298MetfsTer?) c.3736del (p.Asp1246MetfsTer?) c.3667del (p.Asp1223MetfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.33164867C>A | CA363617430 | COL11A2 | n.654G>T c.4848G>T (p.Arg1616Ser) c.4527G>T (p.Arg1509Ser) c.4590G>T (p.Arg1530Ser) n.638G>T c.4002G>T (p.Arg1334Ser) c.4134G>T (p.Arg1378Ser) c.3954G>T (p.Arg1318Ser) c.3891G>T (p.Arg1297Ser) c.3735G>T (p.Arg1245Ser) c.3666G>T (p.Arg1222Ser) | gnomAD v4 |
| 6 | g.33164867C>G | CA363617428 | COL11A2 | n.654G>C c.4848G>C (p.Arg1616Ser) c.4527G>C (p.Arg1509Ser) c.4590G>C (p.Arg1530Ser) n.638G>C c.4002G>C (p.Arg1334Ser) c.4134G>C (p.Arg1378Ser) c.3954G>C (p.Arg1318Ser) c.3891G>C (p.Arg1297Ser) c.3735G>C (p.Arg1245Ser) c.3666G>C (p.Arg1222Ser) | |
| 6 | g.33164867C>T | CA449867248 | COL11A2 | n.654G>A c.4848G>A (p.Arg1616=) c.4527G>A (p.Arg1509=) c.4590G>A (p.Arg1530=) n.638G>A c.4002G>A (p.Arg1334=) c.4134G>A (p.Arg1378=) c.3954G>A (p.Arg1318=) c.3891G>A (p.Arg1297=) c.3735G>A (p.Arg1245=) c.3666G>A (p.Arg1222=) | |
| 6 | g.33164868C>A | CA363617432 | COL11A2 | n.653G>T c.4847G>T (p.Arg1616Met) c.4526G>T (p.Arg1509Met) c.4589G>T (p.Arg1530Met) n.637G>T c.4001G>T (p.Arg1334Met) c.4133G>T (p.Arg1378Met) c.3953G>T (p.Arg1318Met) c.3890G>T (p.Arg1297Met) c.3734G>T (p.Arg1245Met) c.3665G>T (p.Arg1222Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.33164868C= | CA1619890441 | COL11A2 | n.653G= c.4847G= (p.Arg1616=) c.4526G= (p.Arg1509=) c.4589G= (p.Arg1530=) n.637G= c.4001G= (p.Arg1334=) c.4133G= (p.Arg1378=) c.3953G= (p.Arg1318=) c.3890G= (p.Arg1297=) c.3734G= (p.Arg1245=) c.3665G= (p.Arg1222=) | |
| 6 | g.33164868C>G | CA363617436 | COL11A2 | n.653G>C c.4847G>C (p.Arg1616Thr) c.4526G>C (p.Arg1509Thr) c.4589G>C (p.Arg1530Thr) n.637G>C c.4001G>C (p.Arg1334Thr) c.4133G>C (p.Arg1378Thr) c.3953G>C (p.Arg1318Thr) c.3890G>C (p.Arg1297Thr) c.3734G>C (p.Arg1245Thr) c.3665G>C (p.Arg1222Thr) |