Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.79984830_79984831delinsCA | CA1471255348 | ANTXR2 | c.1074_1075delinsTG (p.Pro358=) c.843_844delinsTG (p.Pro281=) c.765_766delinsTG (p.Pro255=) c.*224_*225delinsTG (n.*224_*225delinsTG) | |
4 | g.79984831del | CA2981725 | ANTXR2 | c.1074del (p.Ala359HisfsTer?) c.843del (p.Ala282HisfsTer?) c.765del (p.Ala256HisfsTer?) c.*224del (n.*224del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984831A= | CA1471255362 | ANTXR2 | c.1074T= (p.Pro358=) c.843T= (p.Pro281=) c.765T= (p.Pro255=) c.*224T= (n.*224T=) | |
4 | g.79984831A>C | CA2981729 | ANTXR2 | c.1074T>G (p.Pro358=) c.843T>G (p.Pro281=) c.765T>G (p.Pro255=) c.*224T>G (n.*224T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.79984831A>G | CA440062369 | ANTXR2 | c.1074T>C (p.Pro358=) c.843T>C (p.Pro281=) c.765T>C (p.Pro255=) c.*224T>C (n.*224T>C) | dbSNP gnomAD v4 |
4 | g.79984831A>T | CA2981728 | ANTXR2 | c.1074T>A (p.Pro358=) c.843T>A (p.Pro281=) c.765T>A (p.Pro255=) c.*224T>A (n.*224T>A) | dbSNP ExAC gnomAD v4 |
4 | g.79984831dup | CA552730605 | ANTXR2 | c.1074dup (p.Ala359CysfsTer13) c.843dup (p.Ala282CysfsTer13) c.765dup (p.Ala256CysfsTer13) c.*224dup (n.*224dup) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984832G>A | CA357471629 | ANTXR2 | c.1073C>T (p.Pro358Leu) c.842C>T (p.Pro281Leu) c.764C>T (p.Pro255Leu) c.*223C>T (n.*223C>T) | gnomAD v3 gnomAD v4 |
4 | g.79984832G>C | CA357471630 | ANTXR2 | c.1073C>G (p.Pro358Arg) c.842C>G (p.Pro281Arg) c.764C>G (p.Pro255Arg) c.*223C>G (n.*223C>G) | |
4 | g.79984832G>T | CA357471631 | ANTXR2 | c.1073C>A (p.Pro358His) c.842C>A (p.Pro281His) c.764C>A (p.Pro255His) c.*223C>A (n.*223C>A) | |
4 | g.79984835dup | CA252353 | ANTXR2 | c.1073dup (p.Ala359CysfsTer13) c.842dup (p.Ala282CysfsTer13) c.764dup (p.Ala256CysfsTer13) c.*223dup (n.*223dup) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.79984834_79984835dup | CA2981727 | ANTXR2 | c.1072_1073dup (p.Ala359LeufsTer?) c.841_842dup (p.Ala282LeufsTer?) c.763_764dup (p.Ala256LeufsTer?) c.*222_*223dup (n.*222_*223dup) | dbSNP ExAC gnomAD v4 |
4 | g.79984835del | CA2573052361 | ANTXR2 | c.1073del (p.Pro358LeufsTer?) c.842del (p.Pro281LeufsTer?) c.764del (p.Pro255LeufsTer?) c.*223del (n.*223del) | ClinVar dbSNP |
4 | g.79984835_79984839del | CA2546936697 | ANTXR2 | c.1069_1073del (p.Ala357CysfsTer13) c.838_842del (p.Ala280CysfsTer13) c.760_764del (p.Ala254CysfsTer13) c.*219_*223del (n.*219_*223del) | |
4 | g.79984832_79984833insC | CA440062370 | ANTXR2 | c.1072_1073insG (p.Pro358ArgfsTer14) c.841_842insG (p.Pro281ArgfsTer14) c.763_764insG (p.Pro255ArgfsTer14) c.*222_*223insG (n.*222_*223insG) | |
4 | g.79984833G>A | CA357471632 | ANTXR2 | c.1072C>T (p.Pro358Ser) c.841C>T (p.Pro281Ser) c.763C>T (p.Pro255Ser) c.*222C>T (n.*222C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.79984833G>C | CA2981732 | ANTXR2 | c.1072C>G (p.Pro358Ala) c.841C>G (p.Pro281Ala) c.763C>G (p.Pro255Ala) c.*222C>G (n.*222C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984833G= | CA1471255378 | ANTXR2 | c.1072C= (p.Pro358=) c.841C= (p.Pro281=) c.763C= (p.Pro255=) c.*222C= (n.*222C=) | |
4 | g.79984833G>T | CA2981731 | ANTXR2 | c.1072C>A (p.Pro358Thr) c.841C>A (p.Pro281Thr) c.763C>A (p.Pro255Thr) c.*222C>A (n.*222C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984833_79984836delinsGGGC | CA1471255380 | ANTXR2 | c.1069_1072delinsGCCC (p.Ala357=) c.838_841delinsGCCC (p.Ala280=) c.760_763delinsGCCC (p.Ala254=) c.*219_*222delinsGCCC (n.*219_*222delinsGCCC) | |
4 | g.79984836_79984839del | CA2671171163 | ANTXR2 | c.1069_1072del (p.Ala357LeufsTer?) c.838_841del (p.Ala280LeufsTer?) c.760_763del (p.Ala254LeufsTer?) c.*219_*222del (n.*219_*222del) | gnomAD v4 |
4 | g.79984834G>A | CA440062371 | ANTXR2 | c.1071C>T (p.Ala357=) c.840C>T (p.Ala280=) c.762C>T (p.Ala254=) c.*221C>T (n.*221C>T) | gnomAD v4 |
4 | g.79984834G>C | CA440062372 | ANTXR2 | c.1071C>G (p.Ala357=) c.840C>G (p.Ala280=) c.762C>G (p.Ala254=) c.*221C>G (n.*221C>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.79984834G= | CA1471255384 | ANTXR2 | c.1071C= (p.Ala357=) c.840C= (p.Ala280=) c.762C= (p.Ala254=) c.*221C= (n.*221C=) | |
4 | g.79984834G>T | CA440062373 | ANTXR2 | c.1071C>A (p.Ala357=) c.840C>A (p.Ala280=) c.762C>A (p.Ala254=) c.*221C>A (n.*221C>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.79984836_79984838del | CA2981730 | ANTXR2 | c.1069_1071del (p.Ala357del) c.838_840del (p.Ala280del) c.760_762del (p.Ala254del) c.*219_*221del (n.*219_*221del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984834_79984835insT | CA2671171164 | ANTXR2 | c.1070_1071insA (p.Ala359CysfsTer13) c.839_840insA (p.Ala282CysfsTer13) c.761_762insA (p.Ala256CysfsTer13) c.*220_*221insA (n.*220_*221insA) | gnomAD v4 |
4 | g.79984835G>A | CA100495447 | ANTXR2 | c.1070C>T (p.Ala357Val) c.839C>T (p.Ala280Val) c.761C>T (p.Ala254Val) c.*220C>T (n.*220C>T) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.79984835G>C | CA2981735 | ANTXR2 | c.1070C>G (p.Ala357Gly) c.839C>G (p.Ala280Gly) c.761C>G (p.Ala254Gly) c.*220C>G (n.*220C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984835G= | CA1471255389 | ANTXR2 | c.1070C= (p.Ala357=) c.839C= (p.Ala280=) c.761C= (p.Ala254=) c.*220C= (n.*220C=) | |
4 | g.79984835G>T | CA2981734 | ANTXR2 | c.1070C>A (p.Ala357Asp) c.839C>A (p.Ala280Asp) c.761C>A (p.Ala254Asp) c.*220C>A (n.*220C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984835_79984836delinsGC | CA1471255394 | ANTXR2 | c.1069_1070delinsGC (p.Ala357=) c.838_839delinsGC (p.Ala280=) c.760_761delinsGC (p.Ala254=) c.*219_*220delinsGC (n.*219_*220delinsGC) | |
4 | g.79984836_79984837del | CA645521364 | ANTXR2 | c.1069_1070del (p.Ala357ProfsTer14) c.838_839del (p.Ala280ProfsTer14) c.760_761del (p.Ala254ProfsTer14) c.*219_*220del (n.*219_*220del) | gnomAD v4 COSMIC |
4 | g.79984836_79984841del | CA2671171165 | ANTXR2 | c.1065_1070del (p.Pro356_Ala357del) c.834_839del (p.Pro279_Ala280del) c.756_761del (p.Pro253_Ala254del) c.*215_*220del (n.*215_*220del) | gnomAD v4 |
4 | g.79984836del | CA2981733 | ANTXR2 | c.1069del (p.Ala357ProfsTer?) c.838del (p.Ala280ProfsTer?) c.760del (p.Ala254ProfsTer?) c.*219del (n.*219del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.79984836C>A | CA2981738 | ANTXR2 | c.1069G>T (p.Ala357Ser) c.838G>T (p.Ala280Ser) c.760G>T (p.Ala254Ser) c.*219G>T (n.*219G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984836C= | CA1471255411 | ANTXR2 | c.1069G= (p.Ala357=) c.838G= (p.Ala280=) c.760G= (p.Ala254=) c.*219G= (n.*219G=) | |
4 | g.79984836C>G | CA2981736 | ANTXR2 | c.1069G>C (p.Ala357Pro) c.838G>C (p.Ala280Pro) c.760G>C (p.Ala254Pro) c.*219G>C (n.*219G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984836C>T | CA2981737 | ANTXR2 | c.1069G>A (p.Ala357Thr) c.838G>A (p.Ala280Thr) c.760G>A (p.Ala254Thr) c.*219G>A (n.*219G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984836_79984837delinsCG | CA1471255406 | ANTXR2 | c.1068_1069delinsCG (p.Pro356=) c.837_838delinsCG (p.Pro279=) c.759_760delinsCG (p.Pro253=) c.*218_*219delinsCG (n.*218_*219delinsCG) | |
4 | g.79984836_79984837delinsGT | CA100495448 | ANTXR2 | c.1068_1069delinsAC (p.Ala357Pro) c.837_838delinsAC (p.Ala280Pro) c.759_760delinsAC (p.Ala254Pro) c.*218_*219delinsAC (n.*218_*219delinsAC) | dbSNP |
4 | g.79984836_79984869delinsGGGTGGTGGTGGAGGATCCTTAATAACCTGTC | CA645521365 | ANTXR2 | c.1042-6_1069delinsGACAGGTTATTAAGGATCCTCCACCACCACCC c.811-6_838delinsGACAGGTTATTAAGGATCCTCCACCACCACCC c.733-6_760delinsGACAGGTTATTAAGGATCCTCCACCACCACCC c.*192-6_*219delinsGACAGGTTATTAAGGATCCTCCACCACCACCC | COSMIC |
4 | g.79984837G>A | CA2981741 | ANTXR2 | c.1068C>T (p.Pro356=) c.837C>T (p.Pro279=) c.759C>T (p.Pro253=) c.*218C>T (n.*218C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984837G>C | CA2981740 | ANTXR2 | c.1068C>G (p.Pro356=) c.837C>G (p.Pro279=) c.759C>G (p.Pro253=) c.*218C>G (n.*218C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984837G= | CA1471255417 | ANTXR2 | c.1068C= (p.Pro356=) c.837C= (p.Pro279=) c.759C= (p.Pro253=) c.*218C= (n.*218C=) | |
4 | g.79984837G>T | CA2981739 | ANTXR2 | c.1068C>A (p.Pro356=) c.837C>A (p.Pro279=) c.759C>A (p.Pro253=) c.*218C>A (n.*218C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.79984839dup | CA645521366 | ANTXR2 | c.1068dup (p.Ala357ArgfsTer15) c.837dup (p.Ala280ArgfsTer15) c.759dup (p.Ala254ArgfsTer15) c.*218dup (n.*218dup) | COSMIC |
4 | g.79984839del | CA2671171166 | ANTXR2 | c.1068del (p.Ala357ProfsTer?) c.837del (p.Ala280ProfsTer?) c.759del (p.Ala254ProfsTer?) c.*218del (n.*218del) | gnomAD v4 |
4 | g.79984838G>A | CA357471633 | ANTXR2 | c.1067C>T (p.Pro356Leu) c.836C>T (p.Pro279Leu) c.758C>T (p.Pro253Leu) c.*217C>T (n.*217C>T) | gnomAD v4 |
4 | g.79984838G>C | CA357471634 | ANTXR2 | c.1067C>G (p.Pro356Arg) c.836C>G (p.Pro279Arg) c.758C>G (p.Pro253Arg) c.*217C>G (n.*217C>G) | gnomAD v4 |