| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89280224G>A | CA497373432 | ANKRD11 | c.6318C>T (p.Ser2106=) c.*6121C>T (n.*6121C>T) c.745-5033C>T (n.745-5033C>T) c.152-5033C>T c.6216C>T (p.Ser2072=) c.6021C>T (p.Ser2007=) c.6189C>T (p.Ser2063=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89280224G>C | CA397151383 | ANKRD11 | c.6318C>G (p.Ser2106Arg) c.*6121C>G (n.*6121C>G) c.745-5033C>G (n.745-5033C>G) c.152-5033C>G c.6216C>G (p.Ser2072Arg) c.6021C>G (p.Ser2007Arg) c.6189C>G (p.Ser2063Arg) | dbSNP gnomAD v4 |
| 16 | g.89280224G= | CA2241587256 | ANKRD11 | c.6318C= (p.Ser2106=) c.*6121C= (n.*6121C=) c.745-5033C= (n.745-5033C=) c.152-5033C= c.6216C= (p.Ser2072=) c.6021C= (p.Ser2007=) c.6189C= (p.Ser2063=) | |
| 16 | g.89280224G>T | CA397151384 | ANKRD11 | c.6318C>A (p.Ser2106Arg) c.*6121C>A (n.*6121C>A) c.745-5033C>A (n.745-5033C>A) c.152-5033C>A c.6216C>A (p.Ser2072Arg) c.6021C>A (p.Ser2007Arg) c.6189C>A (p.Ser2063Arg) | gnomAD v4 |
| 16 | g.89280225C>A | CA397151385 | ANKRD11 | c.6317G>T (p.Ser2106Ile) c.*6120G>T (n.*6120G>T) c.745-5034G>T (n.745-5034G>T) c.152-5034G>T c.6215G>T (p.Ser2072Ile) c.6020G>T (p.Ser2007Ile) c.6188G>T (p.Ser2063Ile) | |
| 16 | g.89280225C>G | CA397151386 | ANKRD11 | c.6317G>C (p.Ser2106Thr) c.*6120G>C (n.*6120G>C) c.745-5034G>C (n.745-5034G>C) c.152-5034G>C c.6215G>C (p.Ser2072Thr) c.6020G>C (p.Ser2007Thr) c.6188G>C (p.Ser2063Thr) | |
| 16 | g.89280225C>T | CA397151387 | ANKRD11 | c.6317G>A (p.Ser2106Asn) c.*6120G>A (n.*6120G>A) c.745-5034G>A (n.745-5034G>A) c.152-5034G>A c.6215G>A (p.Ser2072Asn) c.6020G>A (p.Ser2007Asn) c.6188G>A (p.Ser2063Asn) | |
| 16 | g.89280226T>A | CA397151388 | ANKRD11 | c.6316A>T (p.Ser2106Cys) c.*6119A>T (n.*6119A>T) c.745-5035A>T (n.745-5035A>T) c.152-5035A>T c.6214A>T (p.Ser2072Cys) c.6019A>T (p.Ser2007Cys) c.6187A>T (p.Ser2063Cys) | |
| 16 | g.89280226T>C | CA397151389 | ANKRD11 | c.6316A>G (p.Ser2106Gly) c.*6119A>G (n.*6119A>G) c.745-5035A>G (n.745-5035A>G) c.152-5035A>G c.6214A>G (p.Ser2072Gly) c.6019A>G (p.Ser2007Gly) c.6187A>G (p.Ser2063Gly) | |
| 16 | g.89280226T>G | CA397151390 | ANKRD11 | c.6316A>C (p.Ser2106Arg) c.*6119A>C (n.*6119A>C) c.745-5035A>C (n.745-5035A>C) c.152-5035A>C c.6214A>C (p.Ser2072Arg) c.6019A>C (p.Ser2007Arg) c.6187A>C (p.Ser2063Arg) | |
| 16 | g.89280227G>A | CA8241499 | ANKRD11 | c.6315C>T (p.Gly2105=) c.*6118C>T (n.*6118C>T) c.745-5036C>T (n.745-5036C>T) c.152-5036C>T c.6213C>T (p.Gly2071=) c.6018C>T (p.Gly2006=) c.6186C>T (p.Gly2062=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89280227G>C | CA497373439 | ANKRD11 | c.6315C>G (p.Gly2105=) c.*6118C>G (n.*6118C>G) c.745-5036C>G (n.745-5036C>G) c.152-5036C>G c.6213C>G (p.Gly2071=) c.6018C>G (p.Gly2006=) c.6186C>G (p.Gly2062=) | |
| 16 | g.89280227G= | CA2241587257 | ANKRD11 | c.6315C= (p.Gly2105=) c.*6118C= (n.*6118C=) c.745-5036C= (n.745-5036C=) c.152-5036C= c.6213C= (p.Gly2071=) c.6018C= (p.Gly2006=) c.6186C= (p.Gly2062=) | |
| 16 | g.89280227G>T | CA497373441 | ANKRD11 | c.6315C>A (p.Gly2105=) c.*6118C>A (n.*6118C>A) c.745-5036C>A (n.745-5036C>A) c.152-5036C>A c.6213C>A (p.Gly2071=) c.6018C>A (p.Gly2006=) c.6186C>A (p.Gly2062=) | dbSNP gnomAD v2 |
| 16 | g.89280228C>A | CA397151393 | ANKRD11 | c.6314G>T (p.Gly2105Val) c.*6117G>T (n.*6117G>T) c.745-5037G>T (n.745-5037G>T) c.152-5037G>T c.6212G>T (p.Gly2071Val) c.6017G>T (p.Gly2006Val) c.6185G>T (p.Gly2062Val) | |
| 16 | g.89280228C>G | CA397151391 | ANKRD11 | c.6314G>C (p.Gly2105Ala) c.*6117G>C (n.*6117G>C) c.745-5037G>C (n.745-5037G>C) c.152-5037G>C c.6212G>C (p.Gly2071Ala) c.6017G>C (p.Gly2006Ala) c.6185G>C (p.Gly2062Ala) | |
| 16 | g.89280228C>T | CA397151392 | ANKRD11 | c.6314G>A (p.Gly2105Asp) c.*6117G>A (n.*6117G>A) c.745-5037G>A (n.745-5037G>A) c.152-5037G>A c.6212G>A (p.Gly2071Asp) c.6017G>A (p.Gly2006Asp) c.6185G>A (p.Gly2062Asp) | gnomAD v4 |
| 16 | g.89280229C>A | CA397151394 | ANKRD11 | c.6313G>T (p.Gly2105Cys) c.*6116G>T (n.*6116G>T) c.745-5038G>T (n.745-5038G>T) c.152-5038G>T c.6211G>T (p.Gly2071Cys) c.6016G>T (p.Gly2006Cys) c.6184G>T (p.Gly2062Cys) | |
| 16 | g.89280229C= | CA2241587258 | ANKRD11 | c.6313G= (p.Gly2105=) c.*6116G= (n.*6116G=) c.745-5038G= (n.745-5038G=) c.152-5038G= c.6211G= (p.Gly2071=) c.6016G= (p.Gly2006=) c.6184G= (p.Gly2062=) | |
| 16 | g.89280229C>G | CA397151395 | ANKRD11 | c.6313G>C (p.Gly2105Arg) c.*6116G>C (n.*6116G>C) c.745-5038G>C (n.745-5038G>C) c.152-5038G>C c.6211G>C (p.Gly2071Arg) c.6016G>C (p.Gly2006Arg) c.6184G>C (p.Gly2062Arg) | gnomAD v4 |
| 16 | g.89280229C>T | CA8241500 | ANKRD11 | c.6313G>A (p.Gly2105Ser) c.*6116G>A (n.*6116G>A) c.745-5038G>A (n.745-5038G>A) c.152-5038G>A c.6211G>A (p.Gly2071Ser) c.6016G>A (p.Gly2006Ser) c.6184G>A (p.Gly2062Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89280230G>A | CA8241501 | ANKRD11 | c.6312C>T (p.Asp2104=) c.*6115C>T (n.*6115C>T) c.745-5039C>T (n.745-5039C>T) c.152-5039C>T c.6210C>T (p.Asp2070=) c.6015C>T (p.Asp2005=) c.6183C>T (p.Asp2061=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89280230G>C | CA397151396 | ANKRD11 | c.6312C>G (p.Asp2104Glu) c.*6115C>G (n.*6115C>G) c.745-5039C>G (n.745-5039C>G) c.152-5039C>G c.6210C>G (p.Asp2070Glu) c.6015C>G (p.Asp2005Glu) c.6183C>G (p.Asp2061Glu) | |
| 16 | g.89280230G= | CA2241587259 | ANKRD11 | c.6312C= (p.Asp2104=) c.*6115C= (n.*6115C=) c.745-5039C= (n.745-5039C=) c.152-5039C= c.6210C= (p.Asp2070=) c.6015C= (p.Asp2005=) c.6183C= (p.Asp2061=) | |
| 16 | g.89280230G>T | CA397151397 | ANKRD11 | c.6312C>A (p.Asp2104Glu) c.*6115C>A (n.*6115C>A) c.745-5039C>A (n.745-5039C>A) c.152-5039C>A c.6210C>A (p.Asp2070Glu) c.6015C>A (p.Asp2005Glu) c.6183C>A (p.Asp2061Glu) | gnomAD v4 |
| 16 | g.89280231T>A | CA397151398 | ANKRD11 | c.6311A>T (p.Asp2104Val) c.*6114A>T (n.*6114A>T) c.745-5040A>T (n.745-5040A>T) c.152-5040A>T c.6209A>T (p.Asp2070Val) c.6014A>T (p.Asp2005Val) c.6182A>T (p.Asp2061Val) | |
| 16 | g.89280231T>C | CA397151399 | ANKRD11 | c.6311A>G (p.Asp2104Gly) c.*6114A>G (n.*6114A>G) c.745-5040A>G (n.745-5040A>G) c.152-5040A>G c.6209A>G (p.Asp2070Gly) c.6014A>G (p.Asp2005Gly) c.6182A>G (p.Asp2061Gly) | dbSNP |
| 16 | g.89280231T>G | CA397151400 | ANKRD11 | c.6311A>C (p.Asp2104Ala) c.*6114A>C (n.*6114A>C) c.745-5040A>C (n.745-5040A>C) c.152-5040A>C c.6209A>C (p.Asp2070Ala) c.6014A>C (p.Asp2005Ala) c.6182A>C (p.Asp2061Ala) | |
| 16 | g.89280232C>A | CA397151401 | ANKRD11 | c.6310G>T (p.Asp2104Tyr) c.*6113G>T (n.*6113G>T) c.745-5041G>T (n.745-5041G>T) c.152-5041G>T c.6208G>T (p.Asp2070Tyr) c.6013G>T (p.Asp2005Tyr) c.6181G>T (p.Asp2061Tyr) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89280232C= | CA2241587260 | ANKRD11 | c.6310G= (p.Asp2104=) c.*6113G= (n.*6113G=) c.745-5041G= (n.745-5041G=) c.152-5041G= c.6208G= (p.Asp2070=) c.6013G= (p.Asp2005=) c.6181G= (p.Asp2061=) | |
| 16 | g.89280232C>G | CA397151402 | ANKRD11 | c.6310G>C (p.Asp2104His) c.*6113G>C (n.*6113G>C) c.745-5041G>C (n.745-5041G>C) c.152-5041G>C c.6208G>C (p.Asp2070His) c.6013G>C (p.Asp2005His) c.6181G>C (p.Asp2061His) | |
| 16 | g.89280232C>T | CA397151403 | ANKRD11 | c.6310G>A (p.Asp2104Asn) c.*6113G>A (n.*6113G>A) c.745-5041G>A (n.745-5041G>A) c.152-5041G>A c.6208G>A (p.Asp2070Asn) c.6013G>A (p.Asp2005Asn) c.6181G>A (p.Asp2061Asn) | gnomAD v4 |
| 16 | g.89280233C>A | CA497373446 | ANKRD11 | c.6309G>T (p.Leu2103=) c.*6112G>T (n.*6112G>T) c.745-5042G>T (n.745-5042G>T) c.152-5042G>T c.6207G>T (p.Leu2069=) c.6012G>T (p.Leu2004=) c.6180G>T (p.Leu2060=) | |
| 16 | g.89280233C= | CA2241587261 | ANKRD11 | c.6309G= (p.Leu2103=) c.*6112G= (n.*6112G=) c.745-5042G= (n.745-5042G=) c.152-5042G= c.6207G= (p.Leu2069=) c.6012G= (p.Leu2004=) c.6180G= (p.Leu2060=) | |
| 16 | g.89280233C>G | CA497373447 | ANKRD11 | c.6309G>C (p.Leu2103=) c.*6112G>C (n.*6112G>C) c.745-5042G>C (n.745-5042G>C) c.152-5042G>C c.6207G>C (p.Leu2069=) c.6012G>C (p.Leu2004=) c.6180G>C (p.Leu2060=) | |
| 16 | g.89280233C>T | CA497373449 | ANKRD11 | c.6309G>A (p.Leu2103=) c.*6112G>A (n.*6112G>A) c.745-5042G>A (n.745-5042G>A) c.152-5042G>A c.6207G>A (p.Leu2069=) c.6012G>A (p.Leu2004=) c.6180G>A (p.Leu2060=) | dbSNP gnomAD v2 |
| 16 | g.89280234A= | CA2241587262 | ANKRD11 | c.6308T= (p.Leu2103=) c.*6111T= (n.*6111T=) c.745-5043T= (n.745-5043T=) c.152-5043T= c.6206T= (p.Leu2069=) c.6011T= (p.Leu2004=) c.6179T= (p.Leu2060=) | |
| 16 | g.89280234A>C | CA397151406 | ANKRD11 | c.6308T>G (p.Leu2103Arg) c.*6111T>G (n.*6111T>G) c.745-5043T>G (n.745-5043T>G) c.152-5043T>G c.6206T>G (p.Leu2069Arg) c.6011T>G (p.Leu2004Arg) c.6179T>G (p.Leu2060Arg) | |
| 16 | g.89280234A>G | CA397151405 | ANKRD11 | c.6308T>C (p.Leu2103Pro) c.*6111T>C (n.*6111T>C) c.745-5043T>C (n.745-5043T>C) c.152-5043T>C c.6206T>C (p.Leu2069Pro) c.6011T>C (p.Leu2004Pro) c.6179T>C (p.Leu2060Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89280234A>T | CA397151404 | ANKRD11 | c.6308T>A (p.Leu2103Gln) c.*6111T>A (n.*6111T>A) c.745-5043T>A (n.745-5043T>A) c.152-5043T>A c.6206T>A (p.Leu2069Gln) c.6011T>A (p.Leu2004Gln) c.6179T>A (p.Leu2060Gln) | |
| 16 | g.89280235G>A | CA497373451 | ANKRD11 | c.6307C>T (p.Leu2103=) c.*6110C>T (n.*6110C>T) c.745-5044C>T (n.745-5044C>T) c.152-5044C>T c.6205C>T (p.Leu2069=) c.6010C>T (p.Leu2004=) c.6178C>T (p.Leu2060=) | dbSNP gnomAD v4 COSMIC |
| 16 | g.89280235G>C | CA8241502 | ANKRD11 | c.6307C>G (p.Leu2103Val) c.*6110C>G (n.*6110C>G) c.745-5044C>G (n.745-5044C>G) c.152-5044C>G c.6205C>G (p.Leu2069Val) c.6010C>G (p.Leu2004Val) c.6178C>G (p.Leu2060Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89280235G= | CA2241587263 | ANKRD11 | c.6307C= (p.Leu2103=) c.*6110C= (n.*6110C=) c.745-5044C= (n.745-5044C=) c.152-5044C= c.6205C= (p.Leu2069=) c.6010C= (p.Leu2004=) c.6178C= (p.Leu2060=) | |
| 16 | g.89280235G>T | CA397151407 | ANKRD11 | c.6307C>A (p.Leu2103Met) c.*6110C>A (n.*6110C>A) c.745-5044C>A (n.745-5044C>A) c.152-5044C>A c.6205C>A (p.Leu2069Met) c.6010C>A (p.Leu2004Met) c.6178C>A (p.Leu2060Met) | gnomAD v4 |
| 16 | g.89280236G>A | CA8241503 | ANKRD11 | c.6306C>T (p.Phe2102=) c.*6109C>T (n.*6109C>T) c.745-5045C>T (n.745-5045C>T) c.152-5045C>T c.6204C>T (p.Phe2068=) c.6009C>T (p.Phe2003=) c.6177C>T (p.Phe2059=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89280236G>C | CA397151408 | ANKRD11 | c.6306C>G (p.Phe2102Leu) c.*6109C>G (n.*6109C>G) c.745-5045C>G (n.745-5045C>G) c.152-5045C>G c.6204C>G (p.Phe2068Leu) c.6009C>G (p.Phe2003Leu) c.6177C>G (p.Phe2059Leu) | |
| 16 | g.89280236G= | CA2241587264 | ANKRD11 | c.6306C= (p.Phe2102=) c.*6109C= (n.*6109C=) c.745-5045C= (n.745-5045C=) c.152-5045C= c.6204C= (p.Phe2068=) c.6009C= (p.Phe2003=) c.6177C= (p.Phe2059=) | |
| 16 | g.89280236G>T | CA397151409 | ANKRD11 | c.6306C>A (p.Phe2102Leu) c.*6109C>A (n.*6109C>A) c.745-5045C>A (n.745-5045C>A) c.152-5045C>A c.6204C>A (p.Phe2068Leu) c.6009C>A (p.Phe2003Leu) c.6177C>A (p.Phe2059Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89280237A= | CA2241587265 | ANKRD11 | c.6305T= (p.Phe2102=) c.*6108T= (n.*6108T=) c.745-5046T= (n.745-5046T=) c.152-5046T= c.6203T= (p.Phe2068=) c.6008T= (p.Phe2003=) c.6176T= (p.Phe2059=) | |
| 16 | g.89280237A>C | CA397151410 | ANKRD11 | c.6305T>G (p.Phe2102Cys) c.*6108T>G (n.*6108T>G) c.745-5046T>G (n.745-5046T>G) c.152-5046T>G c.6203T>G (p.Phe2068Cys) c.6008T>G (p.Phe2003Cys) c.6176T>G (p.Phe2059Cys) |