| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.156881482_156881537del | CA2697554596 | NTRK1 | c.2051_2106del (p.Arg684LeufsTer?) c.*823_*878del (n.*823_*878del) c.2231_2286del (p.Arg744LeufsTer?) c.290_345del c.2222_2277del (p.Arg741LeufsTer?) c.2213_2268del (p.Arg738LeufsTer?) c.2123_2178del (p.Arg708LeufsTer?) n.2684_2739del n.274_329del | ClinVar |
| 1 | g.156881487_156881516dup | CA889792087 | NTRK1 | c.2056_2085dup (p.Glu695_Val696insLeuGluArgProArgAlaCysProProGlu) c.*828_*857dup (n.*828_*857dup) c.2236_2265dup (p.Glu755_Val756insLeuGluArgProArgAlaCysProProGlu) c.295_324dup c.2227_2256dup (p.Glu752_Val753insLeuGluArgProArgAlaCysProProGlu) c.2218_2247dup (p.Glu749_Val750insLeuGluArgProArgAlaCysProProGlu) c.2128_2157dup (p.Glu719_Val720insLeuGluArgProArgAlaCysProProGlu) n.2689_2718dup n.279_308dup | ClinVar dbSNP |
| 1 | g.156881485A= | CA1200788679 | NTRK1 | c.2054A= (p.Glu685=) c.*826A= (n.*826A=) c.2234A= (p.Glu745=) c.293A= c.2225A= (p.Glu742=) c.2216A= (p.Glu739=) c.2126A= (p.Glu709=) n.2687A= n.277A= | |
| 1 | g.156881485A>C | CA342941412 | NTRK1 | c.2054A>C (p.Glu685Ala) c.*826A>C (n.*826A>C) c.2234A>C (p.Glu745Ala) c.293A>C c.2225A>C (p.Glu742Ala) c.2216A>C (p.Glu739Ala) c.2126A>C (p.Glu709Ala) n.2687A>C n.277A>C | |
| 1 | g.156881485A>G | CA342941416 | NTRK1 | c.2054A>G (p.Glu685Gly) c.*826A>G (n.*826A>G) c.2234A>G (p.Glu745Gly) c.293A>G c.2225A>G (p.Glu742Gly) c.2216A>G (p.Glu739Gly) c.2126A>G (p.Glu709Gly) n.2687A>G n.277A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156881485A>T | CA342941414 | NTRK1 | c.2054A>T (p.Glu685Val) c.*826A>T (n.*826A>T) c.2234A>T (p.Glu745Val) c.293A>T c.2225A>T (p.Glu742Val) c.2216A>T (p.Glu739Val) c.2126A>T (p.Glu709Val) n.2687A>T n.277A>T | dbSNP gnomAD v4 |
| 1 | g.156881486G>A | CA421140608 | NTRK1 | c.2055G>A (p.Glu685=) c.*827G>A (n.*827G>A) c.2235G>A (p.Glu745=) c.294G>A c.2226G>A (p.Glu742=) c.2217G>A (p.Glu739=) c.2127G>A (p.Glu709=) n.2688G>A n.278G>A | |
| 1 | g.156881486G>C | CA342941418 | NTRK1 | c.2055G>C (p.Glu685Asp) c.*827G>C (n.*827G>C) c.2235G>C (p.Glu745Asp) c.294G>C c.2226G>C (p.Glu742Asp) c.2217G>C (p.Glu739Asp) c.2127G>C (p.Glu709Asp) n.2688G>C n.278G>C | |
| 1 | g.156881486G>T | CA342941420 | NTRK1 | c.2055G>T (p.Glu685Asp) c.*827G>T (n.*827G>T) c.2235G>T (p.Glu745Asp) c.294G>T c.2226G>T (p.Glu742Asp) c.2217G>T (p.Glu739Asp) c.2127G>T (p.Glu709Asp) n.2688G>T n.278G>T | |
| 1 | g.156881486_156881487insAAGGATTAAGGC | CA2697514368 | NTRK1 | c.2055_2056insAAGGATTAAGGC c.*827_*828insAAGGATTAAGGC (n.*827_*828insAAGGATTAAGGC) c.2235_2236insAAGGATTAAGGC c.294_295insAAGGATTAAGGC c.2226_2227insAAGGATTAAGGC c.2217_2218insAAGGATTAAGGC c.2127_2128insAAGGATTAAGGC n.2688_2689insAAGGATTAAGGC n.278_279insAAGGATTAAGGC | dbSNP |
| 1 | g.156881487T>A | CA342941421 | NTRK1 | c.2056T>A (p.Leu686Met) c.*828T>A (n.*828T>A) c.2236T>A (p.Leu746Met) c.295T>A c.2227T>A (p.Leu743Met) c.2218T>A (p.Leu740Met) c.2128T>A (p.Leu710Met) n.2689T>A n.279T>A | dbSNP |
| 1 | g.156881487T>C | CA421140609 | NTRK1 | c.2056T>C (p.Leu686=) c.*828T>C (n.*828T>C) c.2236T>C (p.Leu746=) c.295T>C c.2227T>C (p.Leu743=) c.2218T>C (p.Leu740=) c.2128T>C (p.Leu710=) n.2689T>C n.279T>C | |
| 1 | g.156881487T>G | CA342941423 | NTRK1 | c.2056T>G (p.Leu686Val) c.*828T>G (n.*828T>G) c.2236T>G (p.Leu746Val) c.295T>G c.2227T>G (p.Leu743Val) c.2218T>G (p.Leu740Val) c.2128T>G (p.Leu710Val) n.2689T>G n.279T>G | dbSNP |
| 1 | g.156881488T>A | CA342941425 | NTRK1 | c.2057T>A (p.Leu686Ter) c.*829T>A (n.*829T>A) c.2237T>A (p.Leu746Ter) c.296T>A c.2228T>A (p.Leu743Ter) c.2219T>A (p.Leu740Ter) c.2129T>A (p.Leu710Ter) n.2690T>A n.280T>A | |
| 1 | g.156881488T>C | CA342941429 | NTRK1 | c.2057T>C (p.Leu686Ser) c.*829T>C (n.*829T>C) c.2237T>C (p.Leu746Ser) c.296T>C c.2228T>C (p.Leu743Ser) c.2219T>C (p.Leu740Ser) c.2129T>C (p.Leu710Ser) n.2690T>C n.280T>C | |
| 1 | g.156881488T>G | CA342941427 | NTRK1 | c.2057T>G (p.Leu686Trp) c.*829T>G (n.*829T>G) c.2237T>G (p.Leu746Trp) c.296T>G c.2228T>G (p.Leu743Trp) c.2219T>G (p.Leu740Trp) c.2129T>G (p.Leu710Trp) n.2690T>G n.280T>G | |
| 1 | g.156881489G>A | CA421140610 | NTRK1 | c.2058G>A (p.Leu686=) c.*830G>A (n.*830G>A) c.2238G>A (p.Leu746=) c.297G>A c.2229G>A (p.Leu743=) c.2220G>A (p.Leu740=) c.2130G>A (p.Leu710=) n.2691G>A n.281G>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156881489G>C | CA342941431 | NTRK1 | c.2058G>C (p.Leu686Phe) c.*830G>C (n.*830G>C) c.2238G>C (p.Leu746Phe) c.297G>C c.2229G>C (p.Leu743Phe) c.2220G>C (p.Leu740Phe) c.2130G>C (p.Leu710Phe) n.2691G>C n.281G>C | gnomAD v4 |
| 1 | g.156881489G>T | CA342941433 | NTRK1 | c.2058G>T (p.Leu686Phe) c.*830G>T (n.*830G>T) c.2238G>T (p.Leu746Phe) c.297G>T c.2229G>T (p.Leu743Phe) c.2220G>T (p.Leu740Phe) c.2130G>T (p.Leu710Phe) n.2691G>T n.281G>T | dbSNP gnomAD v4 |
| 1 | g.156881489_156881490insTTTTTTAAT | CA1008111756 | NTRK1 | c.2058_2059insTTTTTTAAT (p.Leu686_Glu687insPhePheAsn) c.*830_*831insTTTTTTAAT (n.*830_*831insTTTTTTAAT) c.2238_2239insTTTTTTAAT (p.Leu746_Glu747insPhePheAsn) c.297_298insTTTTTTAAT c.2229_2230insTTTTTTAAT (p.Leu743_Glu744insPhePheAsn) c.2220_2221insTTTTTTAAT (p.Leu740_Glu741insPhePheAsn) c.2130_2131insTTTTTTAAT (p.Leu710_Glu711insPhePheAsn) n.2691_2692insTTTTTTAAT n.281_282insTTTTTTAAT | gnomAD v3 gnomAD v4 |
| 1 | g.156881490G>A | CA342941435 | NTRK1 | c.2059G>A (p.Glu687Lys) c.*831G>A (n.*831G>A) c.2239G>A (p.Glu747Lys) c.298G>A c.2230G>A (p.Glu744Lys) c.2221G>A (p.Glu741Lys) c.2131G>A (p.Glu711Lys) n.2692G>A n.282G>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156881490G>C | CA342941437 | NTRK1 | c.2059G>C (p.Glu687Gln) c.*831G>C (n.*831G>C) c.2239G>C (p.Glu747Gln) c.298G>C c.2230G>C (p.Glu744Gln) c.2221G>C (p.Glu741Gln) c.2131G>C (p.Glu711Gln) n.2692G>C n.282G>C | dbSNP |
| 1 | g.156881490G= | CA1200788683 | NTRK1 | c.2059G= (p.Glu687=) c.*831G= (n.*831G=) c.2239G= (p.Glu747=) c.298G= c.2230G= (p.Glu744=) c.2221G= (p.Glu741=) c.2131G= (p.Glu711=) n.2692G= n.282G= | |
| 1 | g.156881490G>T | CA342941439 | NTRK1 | c.2059G>T (p.Glu687Ter) c.*831G>T (n.*831G>T) c.2239G>T (p.Glu747Ter) c.298G>T c.2230G>T (p.Glu744Ter) c.2221G>T (p.Glu741Ter) c.2131G>T (p.Glu711Ter) n.2692G>T n.282G>T | dbSNP gnomAD v4 |
| 1 | g.156881491A= | CA1200788686 | NTRK1 | c.2060A= (p.Glu687=) c.*832A= (n.*832A=) c.2240A= (p.Glu747=) c.299A= c.2231A= (p.Glu744=) c.2222A= (p.Glu741=) c.2132A= (p.Glu711=) n.2693A= n.283A= | |
| 1 | g.156881491A>C | CA342941447 | NTRK1 | c.2060A>C (p.Glu687Ala) c.*832A>C (n.*832A>C) c.2240A>C (p.Glu747Ala) c.299A>C c.2231A>C (p.Glu744Ala) c.2222A>C (p.Glu741Ala) c.2132A>C (p.Glu711Ala) n.2693A>C n.283A>C | |
| 1 | g.156881491A>G | CA342941449 | NTRK1 | c.2060A>G (p.Glu687Gly) c.*832A>G (n.*832A>G) c.2240A>G (p.Glu747Gly) c.299A>G c.2231A>G (p.Glu744Gly) c.2222A>G (p.Glu741Gly) c.2132A>G (p.Glu711Gly) n.2693A>G n.283A>G | dbSNP gnomAD v4 |
| 1 | g.156881491A>T | CA1169611 | NTRK1 | c.2060A>T (p.Glu687Val) c.*832A>T (n.*832A>T) c.2240A>T (p.Glu747Val) c.299A>T c.2231A>T (p.Glu744Val) c.2222A>T (p.Glu741Val) c.2132A>T (p.Glu711Val) n.2693A>T n.283A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881491_156881492insT | CA1008111759 | NTRK1 | c.2060_2061insT (p.Glu687AspfsTer?) c.*832_*833insT (n.*832_*833insT) c.2240_2241insT (p.Glu747AspfsTer?) c.299_300insT c.2231_2232insT (p.Glu744AspfsTer?) c.2222_2223insT (p.Glu741AspfsTer?) c.2132_2133insT (p.Glu711AspfsTer?) n.2693_2694insT n.283_284insT | gnomAD v3 gnomAD v4 |
| 1 | g.156881492G>A | CA31126014 | NTRK1 | c.2061G>A (p.Glu687=) c.*833G>A (n.*833G>A) c.2241G>A (p.Glu747=) c.300G>A c.2232G>A (p.Glu744=) c.2223G>A (p.Glu741=) c.2133G>A (p.Glu711=) n.2694G>A n.284G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881492G>C | CA342941453 | NTRK1 | c.2061G>C (p.Glu687Asp) c.*833G>C (n.*833G>C) c.2241G>C (p.Glu747Asp) c.300G>C c.2232G>C (p.Glu744Asp) c.2223G>C (p.Glu741Asp) c.2133G>C (p.Glu711Asp) n.2694G>C n.284G>C | dbSNP |
| 1 | g.156881492G= | CA1200788687 | NTRK1 | c.2061G= (p.Glu687=) c.*833G= (n.*833G=) c.2241G= (p.Glu747=) c.300G= c.2232G= (p.Glu744=) c.2223G= (p.Glu741=) c.2133G= (p.Glu711=) n.2694G= n.284G= | |
| 1 | g.156881492G>T | CA342941454 | NTRK1 | c.2061G>T (p.Glu687Asp) c.*833G>T (n.*833G>T) c.2241G>T (p.Glu747Asp) c.300G>T c.2232G>T (p.Glu744Asp) c.2223G>T (p.Glu741Asp) c.2133G>T (p.Glu711Asp) n.2694G>T n.284G>T | |
| 1 | g.156881493C>A | CA421140611 | NTRK1 | c.2062C>A (p.Arg688=) c.*834C>A (n.*834C>A) c.2242C>A (p.Arg748=) c.301C>A c.2233C>A (p.Arg745=) c.2224C>A (p.Arg742=) c.2134C>A (p.Arg712=) n.2695C>A n.285C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881493C= | CA1200788692 | NTRK1 | c.2062C= (p.Arg688=) c.*834C= (n.*834C=) c.2242C= (p.Arg748=) c.301C= c.2233C= (p.Arg745=) c.2224C= (p.Arg742=) c.2134C= (p.Arg712=) n.2695C= n.285C= | |
| 1 | g.156881493C>G | CA342941456 | NTRK1 | c.2062C>G (p.Arg688Gly) c.*834C>G (n.*834C>G) c.2242C>G (p.Arg748Gly) c.301C>G c.2233C>G (p.Arg745Gly) c.2224C>G (p.Arg742Gly) c.2134C>G (p.Arg712Gly) n.2695C>G n.285C>G | dbSNP gnomAD v4 |
| 1 | g.156881493C>T | CA1169612 | NTRK1 | c.2062C>T (p.Arg688Trp) c.*834C>T (n.*834C>T) c.2242C>T (p.Arg748Trp) c.301C>T c.2233C>T (p.Arg745Trp) c.2224C>T (p.Arg742Trp) c.2134C>T (p.Arg712Trp) n.2695C>T n.285C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881494G>A | CA31126027 | NTRK1 | c.2063G>A (p.Arg688Gln) c.*835G>A (n.*835G>A) c.2243G>A (p.Arg748Gln) c.302G>A c.2234G>A (p.Arg745Gln) c.2225G>A (p.Arg742Gln) c.2135G>A (p.Arg712Gln) n.2696G>A n.286G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 1 | g.156881494G>C | CA342941461 | NTRK1 | c.2063G>C (p.Arg688Pro) c.*835G>C (n.*835G>C) c.2243G>C (p.Arg748Pro) c.302G>C c.2234G>C (p.Arg745Pro) c.2225G>C (p.Arg742Pro) c.2135G>C (p.Arg712Pro) n.2696G>C n.286G>C | dbSNP |
| 1 | g.156881494G= | CA1148261562 | NTRK1 | c.2063G= (p.Arg688=) c.*835G= (n.*835G=) c.2243G= (p.Arg748=) c.302G= c.2234G= (p.Arg745=) c.2225G= (p.Arg742=) c.2135G= (p.Arg712=) n.2696G= n.286G= | |
| 1 | g.156881494G>T | CA1169613 | NTRK1 | c.2063G>T (p.Arg688Leu) c.*835G>T (n.*835G>T) c.2243G>T (p.Arg748Leu) c.302G>T c.2234G>T (p.Arg745Leu) c.2225G>T (p.Arg742Leu) c.2135G>T (p.Arg712Leu) n.2696G>T n.286G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881495G>A | CA421140612 | NTRK1 | c.2064G>A (p.Arg688=) c.*836G>A (n.*836G>A) c.2244G>A (p.Arg748=) c.303G>A c.2235G>A (p.Arg745=) c.2226G>A (p.Arg742=) c.2136G>A (p.Arg712=) n.2697G>A n.287G>A | gnomAD v4 |
| 1 | g.156881495G>C | CA421140613 | NTRK1 | c.2064G>C (p.Arg688=) c.*836G>C (n.*836G>C) c.2244G>C (p.Arg748=) c.303G>C c.2235G>C (p.Arg745=) c.2226G>C (p.Arg742=) c.2136G>C (p.Arg712=) n.2697G>C n.287G>C | |
| 1 | g.156881495G>T | CA421140614 | NTRK1 | c.2064G>T (p.Arg688=) c.*836G>T (n.*836G>T) c.2244G>T (p.Arg748=) c.303G>T c.2235G>T (p.Arg745=) c.2226G>T (p.Arg742=) c.2136G>T (p.Arg712=) n.2697G>T n.287G>T | |
| 1 | g.156881496C>A | CA342941468 | NTRK1 | c.2065C>A (p.Pro689Thr) c.*837C>A (n.*837C>A) c.2245C>A (p.Pro749Thr) c.304C>A c.2236C>A (p.Pro746Thr) c.2227C>A (p.Pro743Thr) c.2137C>A (p.Pro713Thr) n.2698C>A n.288C>A | dbSNP gnomAD v4 |
| 1 | g.156881496C>G | CA342941463 | NTRK1 | c.2065C>G (p.Pro689Ala) c.*837C>G (n.*837C>G) c.2245C>G (p.Pro749Ala) c.304C>G c.2236C>G (p.Pro746Ala) c.2227C>G (p.Pro743Ala) c.2137C>G (p.Pro713Ala) n.2698C>G n.288C>G | dbSNP |
| 1 | g.156881496C>T | CA342941466 | NTRK1 | c.2065C>T (p.Pro689Ser) c.*837C>T (n.*837C>T) c.2245C>T (p.Pro749Ser) c.304C>T c.2236C>T (p.Pro746Ser) c.2227C>T (p.Pro743Ser) c.2137C>T (p.Pro713Ser) n.2698C>T n.288C>T | dbSNP |
| 1 | g.156881497C>A | CA342941470 | NTRK1 | c.2066C>A (p.Pro689Gln) c.*838C>A (n.*838C>A) c.2246C>A (p.Pro749Gln) c.305C>A c.2237C>A (p.Pro746Gln) c.2228C>A (p.Pro743Gln) c.2138C>A (p.Pro713Gln) n.2699C>A n.289C>A | gnomAD v4 |
| 1 | g.156881497C>G | CA342941471 | NTRK1 | c.2066C>G (p.Pro689Arg) c.*838C>G (n.*838C>G) c.2246C>G (p.Pro749Arg) c.305C>G c.2237C>G (p.Pro746Arg) c.2228C>G (p.Pro743Arg) c.2138C>G (p.Pro713Arg) n.2699C>G n.289C>G | dbSNP |
| 1 | g.156881497C>T | CA342941473 | NTRK1 | c.2066C>T (p.Pro689Leu) c.*838C>T (n.*838C>T) c.2246C>T (p.Pro749Leu) c.305C>T c.2237C>T (p.Pro746Leu) c.2228C>T (p.Pro743Leu) c.2138C>T (p.Pro713Leu) n.2699C>T n.289C>T | dbSNP COSMIC COSMIC |