UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| 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.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 |
| 1 | g.156881497_156881505del | CA1008111766 | NTRK1 | c.2066_2074del (p.Pro689_Cys692delinsArg) c.*838_*846del (n.*838_*846del) c.2246_2254del (p.Pro749_Cys752delinsArg) c.305_313del c.2237_2245del (p.Pro746_Cys749delinsArg) c.2228_2236del (p.Pro743_Cys746delinsArg) c.2138_2146del (p.Pro713_Cys716delinsArg) n.2699_2707del n.289_297del | gnomAD v3 gnomAD v4 |
| 1 | g.156881498A>C | CA421140615 | NTRK1 | c.2067A>C (p.Pro689=) c.*839A>C (n.*839A>C) c.2247A>C (p.Pro749=) c.306A>C c.2238A>C (p.Pro746=) c.2229A>C (p.Pro743=) c.2139A>C (p.Pro713=) n.2700A>C n.290A>C | dbSNP |
| 1 | g.156881498A>G | CA421140616 | NTRK1 | c.2067A>G (p.Pro689=) c.*839A>G (n.*839A>G) c.2247A>G (p.Pro749=) c.306A>G c.2238A>G (p.Pro746=) c.2229A>G (p.Pro743=) c.2139A>G (p.Pro713=) n.2700A>G n.290A>G | dbSNP |
| 1 | g.156881498A>T | CA421140617 | NTRK1 | c.2067A>T (p.Pro689=) c.*839A>T (n.*839A>T) c.2247A>T (p.Pro749=) c.306A>T c.2238A>T (p.Pro746=) c.2229A>T (p.Pro743=) c.2139A>T (p.Pro713=) n.2700A>T n.290A>T | ClinVar dbSNP |
| 1 | g.156881499C>A | CA342941478 | NTRK1 | c.2068C>A (p.Arg690Ser) c.*840C>A (n.*840C>A) c.2248C>A (p.Arg750Ser) c.307C>A c.2239C>A (p.Arg747Ser) c.2230C>A (p.Arg744Ser) c.2140C>A (p.Arg714Ser) n.2701C>A n.291C>A | dbSNP gnomAD v4 |
| 1 | g.156881499C= | CA1200788703 | NTRK1 | c.2068C= (p.Arg690=) c.*840C= (n.*840C=) c.2248C= (p.Arg750=) c.307C= c.2239C= (p.Arg747=) c.2230C= (p.Arg744=) c.2140C= (p.Arg714=) n.2701C= n.291C= | |
| 1 | g.156881499C>G | CA342941476 | NTRK1 | c.2068C>G (p.Arg690Gly) c.*840C>G (n.*840C>G) c.2248C>G (p.Arg750Gly) c.307C>G c.2239C>G (p.Arg747Gly) c.2230C>G (p.Arg744Gly) c.2140C>G (p.Arg714Gly) n.2701C>G n.291C>G | dbSNP gnomAD v4 |
| 1 | g.156881499C>T | CA31126042 | NTRK1 | c.2068C>T (p.Arg690Cys) c.*840C>T (n.*840C>T) c.2248C>T (p.Arg750Cys) c.307C>T c.2239C>T (p.Arg747Cys) c.2230C>T (p.Arg744Cys) c.2140C>T (p.Arg714Cys) n.2701C>T n.291C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881500G>A | CA1169614 | NTRK1 | c.2069G>A (p.Arg690His) c.*841G>A (n.*841G>A) c.2249G>A (p.Arg750His) c.308G>A c.2240G>A (p.Arg747His) c.2231G>A (p.Arg744His) c.2141G>A (p.Arg714His) n.2702G>A n.292G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 1 | g.156881500G>C | CA342941482 | NTRK1 | c.2069G>C (p.Arg690Pro) c.*841G>C (n.*841G>C) c.2249G>C (p.Arg750Pro) c.308G>C c.2240G>C (p.Arg747Pro) c.2231G>C (p.Arg744Pro) c.2141G>C (p.Arg714Pro) n.2702G>C n.292G>C | dbSNP |
| 1 | g.156881500G= | CA1200788710 | NTRK1 | c.2069G= (p.Arg690=) c.*841G= (n.*841G=) c.2249G= (p.Arg750=) c.308G= c.2240G= (p.Arg747=) c.2231G= (p.Arg744=) c.2141G= (p.Arg714=) n.2702G= n.292G= | |
| 1 | g.156881500G>T | CA342941485 | NTRK1 | c.2069G>T (p.Arg690Leu) c.*841G>T (n.*841G>T) c.2249G>T (p.Arg750Leu) c.308G>T c.2240G>T (p.Arg747Leu) c.2231G>T (p.Arg744Leu) c.2141G>T (p.Arg714Leu) n.2702G>T n.292G>T | |
| 1 | g.156881501T>A | CA421140621 | NTRK1 | c.2070T>A (p.Arg690=) c.*842T>A (n.*842T>A) c.2250T>A (p.Arg750=) c.309T>A c.2241T>A (p.Arg747=) c.2232T>A (p.Arg744=) c.2142T>A (p.Arg714=) n.2703T>A n.293T>A | dbSNP |
| 1 | g.156881501T>C | CA421140623 | NTRK1 | c.2070T>C (p.Arg690=) c.*842T>C (n.*842T>C) c.2250T>C (p.Arg750=) c.309T>C c.2241T>C (p.Arg747=) c.2232T>C (p.Arg744=) c.2142T>C (p.Arg714=) n.2703T>C n.293T>C | dbSNP |
| 1 | g.156881501T>G | CA421140622 | NTRK1 | c.2070T>G (p.Arg690=) c.*842T>G (n.*842T>G) c.2250T>G (p.Arg750=) c.309T>G c.2241T>G (p.Arg747=) c.2232T>G (p.Arg744=) c.2142T>G (p.Arg714=) n.2703T>G n.293T>G | dbSNP |
| 1 | g.156881502G>A | CA342941486 | NTRK1 | c.2071G>A (p.Ala691Thr) c.*843G>A (n.*843G>A) c.2251G>A (p.Ala751Thr) c.310G>A c.2242G>A (p.Ala748Thr) c.2233G>A (p.Ala745Thr) c.2143G>A (p.Ala715Thr) n.2704G>A n.294G>A | dbSNP gnomAD v4 |
| 1 | g.156881502G>C | CA342941488 | NTRK1 | c.2071G>C (p.Ala691Pro) c.*843G>C (n.*843G>C) c.2251G>C (p.Ala751Pro) c.310G>C c.2242G>C (p.Ala748Pro) c.2233G>C (p.Ala745Pro) c.2143G>C (p.Ala715Pro) n.2704G>C n.294G>C | dbSNP |
| 1 | g.156881502G>T | CA342941490 | NTRK1 | c.2071G>T (p.Ala691Ser) c.*843G>T (n.*843G>T) c.2251G>T (p.Ala751Ser) c.310G>T c.2242G>T (p.Ala748Ser) c.2233G>T (p.Ala745Ser) c.2143G>T (p.Ala715Ser) n.2704G>T n.294G>T | dbSNP gnomAD v4 |
| 1 | g.156881503C>A | CA342941492 | NTRK1 | c.2072C>A (p.Ala691Asp) c.*844C>A (n.*844C>A) c.2252C>A (p.Ala751Asp) c.311C>A c.2243C>A (p.Ala748Asp) c.2234C>A (p.Ala745Asp) c.2144C>A (p.Ala715Asp) n.2705C>A n.295C>A | dbSNP gnomAD v4 |
| 1 | g.156881503C= | CA1200788713 | NTRK1 | c.2072C= (p.Ala691=) c.*844C= (n.*844C=) c.2252C= (p.Ala751=) c.311C= c.2243C= (p.Ala748=) c.2234C= (p.Ala745=) c.2144C= (p.Ala715=) n.2705C= n.295C= | |
| 1 | g.156881503C>G | CA342941495 | NTRK1 | c.2072C>G (p.Ala691Gly) c.*844C>G (n.*844C>G) c.2252C>G (p.Ala751Gly) c.311C>G c.2243C>G (p.Ala748Gly) c.2234C>G (p.Ala745Gly) c.2144C>G (p.Ala715Gly) n.2705C>G n.295C>G | dbSNP |
| 1 | g.156881503C>T | CA1169615 | NTRK1 | c.2072C>T (p.Ala691Val) c.*844C>T (n.*844C>T) c.2252C>T (p.Ala751Val) c.311C>T c.2243C>T (p.Ala748Val) c.2234C>T (p.Ala745Val) c.2144C>T (p.Ala715Val) n.2705C>T n.295C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881504C>A | CA421140624 | NTRK1 | c.2073C>A (p.Ala691=) c.*845C>A (n.*845C>A) c.2253C>A (p.Ala751=) c.312C>A c.2244C>A (p.Ala748=) c.2235C>A (p.Ala745=) c.2145C>A (p.Ala715=) n.2706C>A n.296C>A | |
| 1 | g.156881504C>G | CA421140625 | NTRK1 | c.2073C>G (p.Ala691=) c.*845C>G (n.*845C>G) c.2253C>G (p.Ala751=) c.312C>G c.2244C>G (p.Ala748=) c.2235C>G (p.Ala745=) c.2145C>G (p.Ala715=) n.2706C>G n.296C>G | dbSNP gnomAD v4 |
| 1 | g.156881504C>T | CA421140626 | NTRK1 | c.2073C>T (p.Ala691=) c.*845C>T (n.*845C>T) c.2253C>T (p.Ala751=) c.312C>T c.2244C>T (p.Ala748=) c.2235C>T (p.Ala745=) c.2145C>T (p.Ala715=) n.2706C>T n.296C>T | dbSNP gnomAD v4 COSMIC COSMIC |
| 1 | g.156881505T>A | CA342941497 | NTRK1 | c.2074T>A (p.Cys692Ser) c.*846T>A (n.*846T>A) c.2254T>A (p.Cys752Ser) c.313T>A c.2245T>A (p.Cys749Ser) c.2236T>A (p.Cys746Ser) c.2146T>A (p.Cys716Ser) n.2707T>A n.297T>A | dbSNP |
| 1 | g.156881505T>C | CA342941499 | NTRK1 | c.2074T>C (p.Cys692Arg) c.*846T>C (n.*846T>C) c.2254T>C (p.Cys752Arg) c.313T>C c.2245T>C (p.Cys749Arg) c.2236T>C (p.Cys746Arg) c.2146T>C (p.Cys716Arg) n.2707T>C n.297T>C | dbSNP |
| 1 | g.156881505T>G | CA342941502 | NTRK1 | c.2074T>G (p.Cys692Gly) c.*846T>G (n.*846T>G) c.2254T>G (p.Cys752Gly) c.313T>G c.2245T>G (p.Cys749Gly) c.2236T>G (p.Cys746Gly) c.2146T>G (p.Cys716Gly) n.2707T>G n.297T>G | |
| 1 | g.156881506G>A | CA342941504 | NTRK1 | c.2075G>A (p.Cys692Tyr) c.*847G>A (n.*847G>A) c.2255G>A (p.Cys752Tyr) c.314G>A c.2246G>A (p.Cys749Tyr) c.2237G>A (p.Cys746Tyr) c.2147G>A (p.Cys716Tyr) n.2708G>A n.298G>A | gnomAD v4 |
| 1 | g.156881506G>C | CA342941506 | NTRK1 | c.2075G>C (p.Cys692Ser) c.*847G>C (n.*847G>C) c.2255G>C (p.Cys752Ser) c.314G>C c.2246G>C (p.Cys749Ser) c.2237G>C (p.Cys746Ser) c.2147G>C (p.Cys716Ser) n.2708G>C n.298G>C | |
| 1 | g.156881506G>T | CA342941508 | NTRK1 | c.2075G>T (p.Cys692Phe) c.*847G>T (n.*847G>T) c.2255G>T (p.Cys752Phe) c.314G>T c.2246G>T (p.Cys749Phe) c.2237G>T (p.Cys746Phe) c.2147G>T (p.Cys716Phe) n.2708G>T n.298G>T | dbSNP gnomAD v4 |
| 1 | g.156881507C>A | CA342941510 | NTRK1 | c.2076C>A (p.Cys692Ter) c.*848C>A (n.*848C>A) c.2256C>A (p.Cys752Ter) c.315C>A c.2247C>A (p.Cys749Ter) c.2238C>A (p.Cys746Ter) c.2148C>A (p.Cys716Ter) n.2709C>A n.299C>A | gnomAD v3 gnomAD v4 |
| 1 | g.156881507C= | CA1200788715 | NTRK1 | c.2076C= (p.Cys692=) c.*848C= (n.*848C=) c.2256C= (p.Cys752=) c.315C= c.2247C= (p.Cys749=) c.2238C= (p.Cys746=) c.2148C= (p.Cys716=) n.2709C= n.299C= | |
| 1 | g.156881507C>G | CA342941512 | NTRK1 | c.2076C>G (p.Cys692Trp) c.*848C>G (n.*848C>G) c.2256C>G (p.Cys752Trp) c.315C>G c.2247C>G (p.Cys749Trp) c.2238C>G (p.Cys746Trp) c.2148C>G (p.Cys716Trp) n.2709C>G n.299C>G | dbSNP |
| 1 | g.156881507C>T | CA421140628 | NTRK1 | c.2076C>T (p.Cys692=) c.*848C>T (n.*848C>T) c.2256C>T (p.Cys752=) c.315C>T c.2247C>T (p.Cys749=) c.2238C>T (p.Cys746=) c.2148C>T (p.Cys716=) n.2709C>T n.299C>T | dbSNP gnomAD v4 |
| 1 | g.156881507_156881508insT | CA1200788721 | NTRK1 | c.2076_2077insT (p.Pro693SerfsTer?) c.*848_*849insT (n.*848_*849insT) c.2256_2257insT (p.Pro753SerfsTer?) c.315_316insT c.2247_2248insT (p.Pro750SerfsTer?) c.2238_2239insT (p.Pro747SerfsTer?) c.2148_2149insT (p.Pro717SerfsTer?) n.2709_2710insT n.299_300insT | dbSNP |
| 1 | g.156881508C>A | CA342941514 | NTRK1 | c.2077C>A (p.Pro693Thr) c.*849C>A (n.*849C>A) c.2257C>A (p.Pro753Thr) c.316C>A c.2248C>A (p.Pro750Thr) c.2239C>A (p.Pro747Thr) c.2149C>A (p.Pro717Thr) n.2710C>A n.300C>A | dbSNP |
| 1 | g.156881508C= | CA1200788720 | NTRK1 | c.2077C= (p.Pro693=) c.*849C= (n.*849C=) c.2257C= (p.Pro753=) c.316C= c.2248C= (p.Pro750=) c.2239C= (p.Pro747=) c.2149C= (p.Pro717=) n.2710C= n.300C= | |
| 1 | g.156881508C>G | CA342941516 | NTRK1 | c.2077C>G (p.Pro693Ala) c.*849C>G (n.*849C>G) c.2257C>G (p.Pro753Ala) c.316C>G c.2248C>G (p.Pro750Ala) c.2239C>G (p.Pro747Ala) c.2149C>G (p.Pro717Ala) n.2710C>G n.300C>G | dbSNP |
| 1 | g.156881508C>T | CA342941518 | NTRK1 | c.2077C>T (p.Pro693Ser) c.*849C>T (n.*849C>T) c.2257C>T (p.Pro753Ser) c.316C>T c.2248C>T (p.Pro750Ser) c.2239C>T (p.Pro747Ser) c.2149C>T (p.Pro717Ser) n.2710C>T n.300C>T | dbSNP |
| 1 | g.156881509C>A | CA342941524 | NTRK1 | c.2078C>A (p.Pro693Gln) c.*850C>A (n.*850C>A) c.2258C>A (p.Pro753Gln) c.317C>A c.2249C>A (p.Pro750Gln) c.2240C>A (p.Pro747Gln) c.2150C>A (p.Pro717Gln) n.2711C>A n.301C>A | gnomAD v4 |
| 1 | g.156881509C= | CA1200788726 | NTRK1 | c.2078C= (p.Pro693=) c.*850C= (n.*850C=) c.2258C= (p.Pro753=) c.317C= c.2249C= (p.Pro750=) c.2240C= (p.Pro747=) c.2150C= (p.Pro717=) n.2711C= n.301C= | |
| 1 | g.156881509C>G | CA342941523 | NTRK1 | c.2078C>G (p.Pro693Arg) c.*850C>G (n.*850C>G) c.2258C>G (p.Pro753Arg) c.317C>G c.2249C>G (p.Pro750Arg) c.2240C>G (p.Pro747Arg) c.2150C>G (p.Pro717Arg) n.2711C>G n.301C>G | |
| 1 | g.156881509C>T | CA342941520 | NTRK1 | c.2078C>T (p.Pro693Leu) c.*850C>T (n.*850C>T) c.2258C>T (p.Pro753Leu) c.317C>T c.2249C>T (p.Pro750Leu) c.2240C>T (p.Pro747Leu) c.2150C>T (p.Pro717Leu) n.2711C>T n.301C>T | dbSNP |
| 1 | g.156881510A= | CA1148408823 | NTRK1 | c.2079A= (p.Pro693=) c.*851A= (n.*851A=) c.2259A= (p.Pro753=) c.318A= c.2250A= (p.Pro750=) c.2241A= (p.Pro747=) c.2151A= (p.Pro717=) n.2712A= n.302A= | |
| 1 | g.156881510A>C | CA1169617 | NTRK1 | c.2079A>C (p.Pro693=) c.*851A>C (n.*851A>C) c.2259A>C (p.Pro753=) c.318A>C c.2250A>C (p.Pro750=) c.2241A>C (p.Pro747=) c.2151A>C (p.Pro717=) n.2712A>C n.302A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881510A>G | CA1169616 | NTRK1 | c.2079A>G (p.Pro693=) c.*851A>G (n.*851A>G) c.2259A>G (p.Pro753=) c.318A>G c.2250A>G (p.Pro750=) c.2241A>G (p.Pro747=) c.2151A>G (p.Pro717=) n.2712A>G n.302A>G | ClinVar dbSNP ExAC gnomAD v2 |
| 1 | g.156881510A>T | CA421140629 | NTRK1 | c.2079A>T (p.Pro693=) c.*851A>T (n.*851A>T) c.2259A>T (p.Pro753=) c.318A>T c.2250A>T (p.Pro750=) c.2241A>T (p.Pro747=) c.2151A>T (p.Pro717=) n.2712A>T n.302A>T | dbSNP |
| 1 | g.156881510_156881512delinsACC | CA1200788734 | NTRK1 | c.2079_2081delinsACC (p.Pro693=) c.*851_*853delinsACC (n.*851_*853delinsACC) c.2259_2261delinsACC (p.Pro753=) c.318_320delinsACC c.2250_2252delinsACC (p.Pro750=) c.2241_2243delinsACC (p.Pro747=) c.2151_2153delinsACC (p.Pro717=) n.2712_2714delinsACC n.302_304delinsACC | |
| 1 | g.156881511C>A | CA342941527 | NTRK1 | c.2080C>A (p.Pro694Thr) c.*852C>A (n.*852C>A) c.2260C>A (p.Pro754Thr) c.319C>A c.2251C>A (p.Pro751Thr) c.2242C>A (p.Pro748Thr) c.2152C>A (p.Pro718Thr) n.2713C>A n.303C>A | dbSNP |
| 1 | g.156881511C>G | CA342941529 | NTRK1 | c.2080C>G (p.Pro694Ala) c.*852C>G (n.*852C>G) c.2260C>G (p.Pro754Ala) c.319C>G c.2251C>G (p.Pro751Ala) c.2242C>G (p.Pro748Ala) c.2152C>G (p.Pro718Ala) n.2713C>G n.303C>G | dbSNP |
| 1 | g.156881511C>T | CA342941530 | NTRK1 | c.2080C>T (p.Pro694Ser) c.*852C>T (n.*852C>T) c.2260C>T (p.Pro754Ser) c.319C>T c.2251C>T (p.Pro751Ser) c.2242C>T (p.Pro748Ser) c.2152C>T (p.Pro718Ser) n.2713C>T n.303C>T | gnomAD v4 |
| 1 | g.156881511_156881512del | CA1200788736 | NTRK1 | c.2080_2081del (p.Pro694ArgfsTer?) c.*852_*853del (n.*852_*853del) c.2260_2261del (p.Pro754ArgfsTer?) c.319_320del c.2251_2252del (p.Pro751ArgfsTer?) c.2242_2243del (p.Pro748ArgfsTer?) c.2152_2153del (p.Pro718ArgfsTer?) n.2713_2714del n.303_304del | dbSNP |
| 1 | g.156881512C>A | CA342941531 | NTRK1 | c.2081C>A (p.Pro694Gln) c.*853C>A (n.*853C>A) c.2261C>A (p.Pro754Gln) c.320C>A c.2252C>A (p.Pro751Gln) c.2243C>A (p.Pro748Gln) c.2153C>A (p.Pro718Gln) n.2714C>A n.304C>A | gnomAD v4 |
| 1 | g.156881512C>G | CA342941532 | NTRK1 | c.2081C>G (p.Pro694Arg) c.*853C>G (n.*853C>G) c.2261C>G (p.Pro754Arg) c.320C>G c.2252C>G (p.Pro751Arg) c.2243C>G (p.Pro748Arg) c.2153C>G (p.Pro718Arg) n.2714C>G n.304C>G | dbSNP |
| 1 | g.156881512C>T | CA342941533 | NTRK1 | c.2081C>T (p.Pro694Leu) c.*853C>T (n.*853C>T) c.2261C>T (p.Pro754Leu) c.320C>T c.2252C>T (p.Pro751Leu) c.2243C>T (p.Pro748Leu) c.2153C>T (p.Pro718Leu) n.2714C>T n.304C>T | dbSNP gnomAD v4 |
| 1 | g.156881513del | CA1008111772 | NTRK1 | c.2082del (p.Glu695ArgfsTer?) c.*854del (n.*854del) c.2262del (p.Glu755ArgfsTer?) c.321del c.2253del (p.Glu752ArgfsTer?) c.2244del (p.Glu749ArgfsTer?) c.2154del (p.Glu719ArgfsTer?) n.2715del n.305del | gnomAD v3 gnomAD v4 |
| 1 | g.156881513A= | CA1200788739 | NTRK1 | c.2082A= (p.Pro694=) c.*854A= (n.*854A=) c.2262A= (p.Pro754=) c.321A= c.2253A= (p.Pro751=) c.2244A= (p.Pro748=) c.2154A= (p.Pro718=) n.2715A= n.305A= | |
| 1 | g.156881513A>C | CA421140630 | NTRK1 | c.2082A>C (p.Pro694=) c.*854A>C (n.*854A>C) c.2262A>C (p.Pro754=) c.321A>C c.2253A>C (p.Pro751=) c.2244A>C (p.Pro748=) c.2154A>C (p.Pro718=) n.2715A>C n.305A>C | |
| 1 | g.156881513A>G | CA421140631 | NTRK1 | c.2082A>G (p.Pro694=) c.*854A>G (n.*854A>G) c.2262A>G (p.Pro754=) c.321A>G c.2253A>G (p.Pro751=) c.2244A>G (p.Pro748=) c.2154A>G (p.Pro718=) n.2715A>G n.305A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881513A>T | CA421140632 | NTRK1 | c.2082A>T (p.Pro694=) c.*854A>T (n.*854A>T) c.2262A>T (p.Pro754=) c.321A>T c.2253A>T (p.Pro751=) c.2244A>T (p.Pro748=) c.2154A>T (p.Pro718=) n.2715A>T n.305A>T | dbSNP |
| 1 | g.156881514G>A | CA342941534 | NTRK1 | c.2083G>A (p.Glu695Lys) c.*855G>A (n.*855G>A) c.2263G>A (p.Glu755Lys) c.322G>A c.2254G>A (p.Glu752Lys) c.2245G>A (p.Glu749Lys) c.2155G>A (p.Glu719Lys) n.2716G>A n.306G>A | dbSNP |
| 1 | g.156881514G>C | CA342941535 | NTRK1 | c.2083G>C (p.Glu695Gln) c.*855G>C (n.*855G>C) c.2263G>C (p.Glu755Gln) c.322G>C c.2254G>C (p.Glu752Gln) c.2245G>C (p.Glu749Gln) c.2155G>C (p.Glu719Gln) n.2716G>C n.306G>C | dbSNP |
| 1 | g.156881514G>T | CA342941536 | NTRK1 | c.2083G>T (p.Glu695Ter) c.*855G>T (n.*855G>T) c.2263G>T (p.Glu755Ter) c.322G>T c.2254G>T (p.Glu752Ter) c.2245G>T (p.Glu749Ter) c.2155G>T (p.Glu719Ter) n.2716G>T n.306G>T | gnomAD v4 COSMIC COSMIC |
| 1 | g.156881515A= | CA1200788742 | NTRK1 | c.2084A= (p.Glu695=) c.*856A= (n.*856A=) c.2264A= (p.Glu755=) c.323A= c.2255A= (p.Glu752=) c.2246A= (p.Glu749=) c.2156A= (p.Glu719=) n.2717A= n.307A= | |
| 1 | g.156881515A>C | CA342941537 | NTRK1 | c.2084A>C (p.Glu695Ala) c.*856A>C (n.*856A>C) c.2264A>C (p.Glu755Ala) c.323A>C c.2255A>C (p.Glu752Ala) c.2246A>C (p.Glu749Ala) c.2156A>C (p.Glu719Ala) n.2717A>C n.307A>C | |
| 1 | g.156881515A>G | CA342941539 | NTRK1 | c.2084A>G (p.Glu695Gly) c.*856A>G (n.*856A>G) c.2264A>G (p.Glu755Gly) c.323A>G c.2255A>G (p.Glu752Gly) c.2246A>G (p.Glu749Gly) c.2156A>G (p.Glu719Gly) n.2717A>G n.307A>G | dbSNP gnomAD v4 |
| 1 | g.156881515A>T | CA342941540 | NTRK1 | c.2084A>T (p.Glu695Val) c.*856A>T (n.*856A>T) c.2264A>T (p.Glu755Val) c.323A>T c.2255A>T (p.Glu752Val) c.2246A>T (p.Glu749Val) c.2156A>T (p.Glu719Val) n.2717A>T n.307A>T | |
| 1 | g.156881515_156881516insT | CA1200788745 | NTRK1 | c.2084_2085insT (p.Glu695AspfsTer?) c.*856_*857insT (n.*856_*857insT) c.2264_2265insT (p.Glu755AspfsTer?) c.323_324insT c.2255_2256insT (p.Glu752AspfsTer?) c.2246_2247insT (p.Glu749AspfsTer?) c.2156_2157insT (p.Glu719AspfsTer?) n.2717_2718insT n.307_308insT | dbSNP |
| 1 | g.156881516G>A | CA421140633 | NTRK1 | c.2085G>A (p.Glu695=) c.*857G>A (n.*857G>A) c.2265G>A (p.Glu755=) c.324G>A c.2256G>A (p.Glu752=) c.2247G>A (p.Glu749=) c.2157G>A (p.Glu719=) n.2718G>A n.308G>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156881516G>C | CA342941543 | NTRK1 | c.2085G>C (p.Glu695Asp) c.*857G>C (n.*857G>C) c.2265G>C (p.Glu755Asp) c.324G>C c.2256G>C (p.Glu752Asp) c.2247G>C (p.Glu749Asp) c.2157G>C (p.Glu719Asp) n.2718G>C n.308G>C | dbSNP |
| 1 | g.156881516G= | CA1200788746 | NTRK1 | c.2085G= (p.Glu695=) c.*857G= (n.*857G=) c.2265G= (p.Glu755=) c.324G= c.2256G= (p.Glu752=) c.2247G= (p.Glu749=) c.2157G= (p.Glu719=) n.2718G= n.308G= | |
| 1 | g.156881516G>T | CA342941541 | NTRK1 | c.2085G>T (p.Glu695Asp) c.*857G>T (n.*857G>T) c.2265G>T (p.Glu755Asp) c.324G>T c.2256G>T (p.Glu752Asp) c.2247G>T (p.Glu749Asp) c.2157G>T (p.Glu719Asp) n.2718G>T n.308G>T | |
| 1 | g.156881517G>A | CA31126073 | NTRK1 | c.2086G>A (p.Val696Ile) c.*858G>A (n.*858G>A) c.2266G>A (p.Val756Ile) c.325G>A c.2257G>A (p.Val753Ile) c.2248G>A (p.Val750Ile) c.2158G>A (p.Val720Ile) n.2719G>A n.309G>A | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881517G>C | CA342941544 | NTRK1 | c.2086G>C (p.Val696Leu) c.*858G>C (n.*858G>C) c.2266G>C (p.Val756Leu) c.325G>C c.2257G>C (p.Val753Leu) c.2248G>C (p.Val750Leu) c.2158G>C (p.Val720Leu) n.2719G>C n.309G>C | dbSNP |
| 1 | g.156881517G= | CA1200788750 | NTRK1 | c.2086G= (p.Val696=) c.*858G= (n.*858G=) c.2266G= (p.Val756=) c.325G= c.2257G= (p.Val753=) c.2248G= (p.Val750=) c.2158G= (p.Val720=) n.2719G= n.309G= | |
| 1 | g.156881517G>T | CA342941546 | NTRK1 | c.2086G>T (p.Val696Phe) c.*858G>T (n.*858G>T) c.2266G>T (p.Val756Phe) c.325G>T c.2257G>T (p.Val753Phe) c.2248G>T (p.Val750Phe) c.2158G>T (p.Val720Phe) n.2719G>T n.309G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881518T>A | CA342941547 | NTRK1 | c.2087T>A (p.Val696Asp) c.*859T>A (n.*859T>A) c.2267T>A (p.Val756Asp) c.326T>A c.2258T>A (p.Val753Asp) c.2249T>A (p.Val750Asp) c.2159T>A (p.Val720Asp) n.2720T>A n.310T>A | dbSNP |
| 1 | g.156881518T>C | CA342941549 | NTRK1 | c.2087T>C (p.Val696Ala) c.*859T>C (n.*859T>C) c.2267T>C (p.Val756Ala) c.326T>C c.2258T>C (p.Val753Ala) c.2249T>C (p.Val750Ala) c.2159T>C (p.Val720Ala) n.2720T>C n.310T>C | dbSNP |
| 1 | g.156881518T>G | CA342941550 | NTRK1 | c.2087T>G (p.Val696Gly) c.*859T>G (n.*859T>G) c.2267T>G (p.Val756Gly) c.326T>G c.2258T>G (p.Val753Gly) c.2249T>G (p.Val750Gly) c.2159T>G (p.Val720Gly) n.2720T>G n.310T>G | dbSNP |
| 1 | g.156881519C>A | CA421140634 | NTRK1 | c.2088C>A (p.Val696=) c.*860C>A (n.*860C>A) c.2268C>A (p.Val756=) c.327C>A c.2259C>A (p.Val753=) c.2250C>A (p.Val750=) c.2160C>A (p.Val720=) n.2721C>A n.311C>A | dbSNP |
| 1 | g.156881519C= | CA1200788754 | NTRK1 | c.2088C= (p.Val696=) c.*860C= (n.*860C=) c.2268C= (p.Val756=) c.327C= c.2259C= (p.Val753=) c.2250C= (p.Val750=) c.2160C= (p.Val720=) n.2721C= n.311C= | |
| 1 | g.156881519C>G | CA421140635 | NTRK1 | c.2088C>G (p.Val696=) c.*860C>G (n.*860C>G) c.2268C>G (p.Val756=) c.327C>G c.2259C>G (p.Val753=) c.2250C>G (p.Val750=) c.2160C>G (p.Val720=) n.2721C>G n.311C>G | dbSNP |
| 1 | g.156881519C>T | CA1169618 | NTRK1 | c.2088C>T (p.Val696=) c.*860C>T (n.*860C>T) c.2268C>T (p.Val756=) c.327C>T c.2259C>T (p.Val753=) c.2250C>T (p.Val750=) c.2160C>T (p.Val720=) n.2721C>T n.311C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881520T>A | CA342941552 | NTRK1 | c.2089T>A (p.Tyr697Asn) c.*861T>A (n.*861T>A) c.2269T>A (p.Tyr757Asn) c.328T>A c.2260T>A (p.Tyr754Asn) c.2251T>A (p.Tyr751Asn) c.2161T>A (p.Tyr721Asn) n.2722T>A n.312T>A | |
| 1 | g.156881520T>C | CA342941553 | NTRK1 | c.2089T>C (p.Tyr697His) c.*861T>C (n.*861T>C) c.2269T>C (p.Tyr757His) c.328T>C c.2260T>C (p.Tyr754His) c.2251T>C (p.Tyr751His) c.2161T>C (p.Tyr721His) n.2722T>C n.312T>C | |
| 1 | g.156881520T>G | CA342941554 | NTRK1 | c.2089T>G (p.Tyr697Asp) c.*861T>G (n.*861T>G) c.2269T>G (p.Tyr757Asp) c.328T>G c.2260T>G (p.Tyr754Asp) c.2251T>G (p.Tyr751Asp) c.2161T>G (p.Tyr721Asp) n.2722T>G n.312T>G | |
| 1 | g.156881521A= | CA1200788758 | NTRK1 | c.2090A= (p.Tyr697=) c.*862A= (n.*862A=) c.2270A= (p.Tyr757=) c.329A= c.2261A= (p.Tyr754=) c.2252A= (p.Tyr751=) c.2162A= (p.Tyr721=) n.2723A= n.313A= | |
| 1 | g.156881521A>C | CA342941555 | NTRK1 | c.2090A>C (p.Tyr697Ser) c.*862A>C (n.*862A>C) c.2270A>C (p.Tyr757Ser) c.329A>C c.2261A>C (p.Tyr754Ser) c.2252A>C (p.Tyr751Ser) c.2162A>C (p.Tyr721Ser) n.2723A>C n.313A>C | dbSNP |
| 1 | g.156881521A>G | CA342941556 | NTRK1 | c.2090A>G (p.Tyr697Cys) c.*862A>G (n.*862A>G) c.2270A>G (p.Tyr757Cys) c.329A>G c.2261A>G (p.Tyr754Cys) c.2252A>G (p.Tyr751Cys) c.2162A>G (p.Tyr721Cys) n.2723A>G n.313A>G | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881521A>T | CA342941557 | NTRK1 | c.2090A>T (p.Tyr697Phe) c.*862A>T (n.*862A>T) c.2270A>T (p.Tyr757Phe) c.329A>T c.2261A>T (p.Tyr754Phe) c.2252A>T (p.Tyr751Phe) c.2162A>T (p.Tyr721Phe) n.2723A>T n.313A>T | dbSNP |
| 1 | g.156881522C>A | CA342941558 | NTRK1 | c.2091C>A (p.Tyr697Ter) c.*863C>A (n.*863C>A) c.2271C>A (p.Tyr757Ter) c.330C>A c.2262C>A (p.Tyr754Ter) c.2253C>A (p.Tyr751Ter) c.2163C>A (p.Tyr721Ter) n.2724C>A n.314C>A | |
| 1 | g.156881522C= | CA1141811548 | NTRK1 | c.2091C= (p.Tyr697=) c.*863C= (n.*863C=) c.2271C= (p.Tyr757=) c.330C= c.2262C= (p.Tyr754=) c.2253C= (p.Tyr751=) c.2163C= (p.Tyr721=) n.2724C= n.314C= | |
| 1 | g.156881522C>G | CA342941559 | NTRK1 | c.2091C>G (p.Tyr697Ter) c.*863C>G (n.*863C>G) c.2271C>G (p.Tyr757Ter) c.330C>G c.2262C>G (p.Tyr754Ter) c.2253C>G (p.Tyr751Ter) c.2163C>G (p.Tyr721Ter) n.2724C>G n.314C>G | ClinVar dbSNP |
| 1 | g.156881522C>T | CA1169619 | NTRK1 | c.2091C>T (p.Tyr697=) c.*863C>T (n.*863C>T) c.2271C>T (p.Tyr757=) c.330C>T c.2262C>T (p.Tyr754=) c.2253C>T (p.Tyr751=) c.2163C>T (p.Tyr721=) n.2724C>T n.314C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881523G>A | CA1169620 | NTRK1 | c.2092G>A (p.Ala698Thr) c.*864G>A (n.*864G>A) c.2272G>A (p.Ala758Thr) c.331G>A c.2263G>A (p.Ala755Thr) c.2254G>A (p.Ala752Thr) c.2164G>A (p.Ala722Thr) n.2725G>A n.315G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881523G>C | CA342941561 | NTRK1 | c.2092G>C (p.Ala698Pro) c.*864G>C (n.*864G>C) c.2272G>C (p.Ala758Pro) c.331G>C c.2263G>C (p.Ala755Pro) c.2254G>C (p.Ala752Pro) c.2164G>C (p.Ala722Pro) n.2725G>C n.315G>C | dbSNP |
| 1 | g.156881523G= | CA1140762817 | NTRK1 | c.2092G= (p.Ala698=) c.*864G= (n.*864G=) c.2272G= (p.Ala758=) c.331G= c.2263G= (p.Ala755=) c.2254G= (p.Ala752=) c.2164G= (p.Ala722=) n.2725G= n.315G= | |
| 1 | g.156881523G>T | CA342941560 | NTRK1 | c.2092G>T (p.Ala698Ser) c.*864G>T (n.*864G>T) c.2272G>T (p.Ala758Ser) c.331G>T c.2263G>T (p.Ala755Ser) c.2254G>T (p.Ala752Ser) c.2164G>T (p.Ala722Ser) n.2725G>T n.315G>T | gnomAD v4 |
| 1 | g.156881524C>A | CA342941563 | NTRK1 | c.2093C>A (p.Ala698Asp) c.*865C>A (n.*865C>A) c.2273C>A (p.Ala758Asp) c.332C>A c.2264C>A (p.Ala755Asp) c.2255C>A (p.Ala752Asp) c.2165C>A (p.Ala722Asp) n.2726C>A n.316C>A | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881524C= | CA1200788767 | NTRK1 | c.2093C= (p.Ala698=) c.*865C= (n.*865C=) c.2273C= (p.Ala758=) c.332C= c.2264C= (p.Ala755=) c.2255C= (p.Ala752=) c.2165C= (p.Ala722=) n.2726C= n.316C= | |
| 1 | g.156881524C>G | CA342941565 | NTRK1 | c.2093C>G (p.Ala698Gly) c.*865C>G (n.*865C>G) c.2273C>G (p.Ala758Gly) c.332C>G c.2264C>G (p.Ala755Gly) c.2255C>G (p.Ala752Gly) c.2165C>G (p.Ala722Gly) n.2726C>G n.316C>G | dbSNP |
| 1 | g.156881524C>T | CA342941564 | NTRK1 | c.2093C>T (p.Ala698Val) c.*865C>T (n.*865C>T) c.2273C>T (p.Ala758Val) c.332C>T c.2264C>T (p.Ala755Val) c.2255C>T (p.Ala752Val) c.2165C>T (p.Ala722Val) n.2726C>T n.316C>T | dbSNP |
| 1 | g.156881525C>A | CA421140636 | NTRK1 | c.2094C>A (p.Ala698=) c.*866C>A (n.*866C>A) c.2274C>A (p.Ala758=) c.333C>A c.2265C>A (p.Ala755=) c.2256C>A (p.Ala752=) c.2166C>A (p.Ala722=) n.2727C>A n.317C>A | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156881525C= | CA1200788770 | NTRK1 | c.2094C= (p.Ala698=) c.*866C= (n.*866C=) c.2274C= (p.Ala758=) c.333C= c.2265C= (p.Ala755=) c.2256C= (p.Ala752=) c.2166C= (p.Ala722=) n.2727C= n.317C= | |
| 1 | g.156881525C>G | CA1169621 | NTRK1 | c.2094C>G (p.Ala698=) c.*866C>G (n.*866C>G) c.2274C>G (p.Ala758=) c.333C>G c.2265C>G (p.Ala755=) c.2256C>G (p.Ala752=) c.2166C>G (p.Ala722=) n.2727C>G n.317C>G | ClinVar dbSNP ExAC gnomAD v2 |
| 1 | g.156881525C>T | CA421140637 | NTRK1 | c.2094C>T (p.Ala698=) c.*866C>T (n.*866C>T) c.2274C>T (p.Ala758=) c.333C>T c.2265C>T (p.Ala755=) c.2256C>T (p.Ala752=) c.2166C>T (p.Ala722=) n.2727C>T n.317C>T | dbSNP |
| 1 | g.156881525_156881526delinsCA | CA1200788771 | NTRK1 | c.2094_2095delinsCA (p.Ala698=) c.*866_*867delinsCA (n.*866_*867delinsCA) c.2274_2275delinsCA (p.Ala758=) c.333_334delinsCA c.2265_2266delinsCA (p.Ala755=) c.2256_2257delinsCA (p.Ala752=) c.2166_2167delinsCA (p.Ala722=) n.2727_2728delinsCA n.317_318delinsCA | |
| 1 | g.156881526del | CA1008111783 | NTRK1 | c.2095del (p.Ile699SerfsTer?) c.*867del (n.*867del) c.2275del (p.Ile759SerfsTer?) c.334del c.2266del (p.Ile756SerfsTer?) c.2257del (p.Ile753SerfsTer?) c.2167del (p.Ile723SerfsTer?) n.2728del n.318del | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881526A>C | CA342941569 | NTRK1 | c.2095A>C (p.Ile699Leu) c.*867A>C (n.*867A>C) c.2275A>C (p.Ile759Leu) c.334A>C c.2266A>C (p.Ile756Leu) c.2257A>C (p.Ile753Leu) c.2167A>C (p.Ile723Leu) n.2728A>C n.318A>C | dbSNP |
| 1 | g.156881526A>G | CA342941566 | NTRK1 | c.2095A>G (p.Ile699Val) c.*867A>G (n.*867A>G) c.2275A>G (p.Ile759Val) c.334A>G c.2266A>G (p.Ile756Val) c.2257A>G (p.Ile753Val) c.2167A>G (p.Ile723Val) n.2728A>G n.318A>G | |
| 1 | g.156881526A>T | CA342941568 | NTRK1 | c.2095A>T (p.Ile699Phe) c.*867A>T (n.*867A>T) c.2275A>T (p.Ile759Phe) c.334A>T c.2266A>T (p.Ile756Phe) c.2257A>T (p.Ile753Phe) c.2167A>T (p.Ile723Phe) n.2728A>T n.318A>T | dbSNP |
| 1 | g.156881527T>A | CA342941570 | NTRK1 | c.2096T>A (p.Ile699Asn) c.*868T>A (n.*868T>A) c.2276T>A (p.Ile759Asn) c.335T>A c.2267T>A (p.Ile756Asn) c.2258T>A (p.Ile753Asn) c.2168T>A (p.Ile723Asn) n.2729T>A n.319T>A | dbSNP |
| 1 | g.156881527T>C | CA342941571 | NTRK1 | c.2096T>C (p.Ile699Thr) c.*868T>C (n.*868T>C) c.2276T>C (p.Ile759Thr) c.335T>C c.2267T>C (p.Ile756Thr) c.2258T>C (p.Ile753Thr) c.2168T>C (p.Ile723Thr) n.2729T>C n.319T>C | dbSNP |
| 1 | g.156881527T>G | CA342941572 | NTRK1 | c.2096T>G (p.Ile699Ser) c.*868T>G (n.*868T>G) c.2276T>G (p.Ile759Ser) c.335T>G c.2267T>G (p.Ile756Ser) c.2258T>G (p.Ile753Ser) c.2168T>G (p.Ile723Ser) n.2729T>G n.319T>G | |
| 1 | g.156881527T= | CA1200788776 | NTRK1 | c.2096T= (p.Ile699=) c.*868T= (n.*868T=) c.2276T= (p.Ile759=) c.335T= c.2267T= (p.Ile756=) c.2258T= (p.Ile753=) c.2168T= (p.Ile723=) n.2729T= n.319T= | |
| 1 | g.156881528C>A | CA31126111 | NTRK1 | c.2097C>A (p.Ile699=) c.*869C>A (n.*869C>A) c.2277C>A (p.Ile759=) c.336C>A c.2268C>A (p.Ile756=) c.2259C>A (p.Ile753=) c.2169C>A (p.Ile723=) n.2730C>A n.320C>A | dbSNP |
| 1 | g.156881528C= | CA1140614598 | NTRK1 | c.2097C= (p.Ile699=) c.*869C= (n.*869C=) c.2277C= (p.Ile759=) c.336C= c.2268C= (p.Ile756=) c.2259C= (p.Ile753=) c.2169C= (p.Ile723=) n.2730C= n.320C= | |
| 1 | g.156881528C>G | CA31126113 | NTRK1 | c.2097C>G (p.Ile699Met) c.*869C>G (n.*869C>G) c.2277C>G (p.Ile759Met) c.336C>G c.2268C>G (p.Ile756Met) c.2259C>G (p.Ile753Met) c.2169C>G (p.Ile723Met) n.2730C>G n.320C>G | dbSNP |
| 1 | g.156881528C>T | CA421140638 | NTRK1 | c.2097C>T (p.Ile699=) c.*869C>T (n.*869C>T) c.2277C>T (p.Ile759=) c.336C>T c.2268C>T (p.Ile756=) c.2259C>T (p.Ile753=) c.2169C>T (p.Ile723=) n.2730C>T n.320C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156881528_156881529insTGCTGCTGGC | CA1008111790 | NTRK1 | c.2097_2098insTGCTGCTGGC (p.Met700CysfsTer?) c.*869_*870insTGCTGCTGGC (n.*869_*870insTGCTGCTGGC) c.2277_2278insTGCTGCTGGC (p.Met760CysfsTer?) c.336_337insTGCTGCTGGC c.2268_2269insTGCTGCTGGC (p.Met757CysfsTer?) c.2259_2260insTGCTGCTGGC (p.Met754CysfsTer?) c.2169_2170insTGCTGCTGGC (p.Met724CysfsTer?) n.2730_2731insTGCTGCTGGC n.320_321insTGCTGCTGGC | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881529A>C | CA342941574 | NTRK1 | c.2098A>C (p.Met700Leu) c.*870A>C (n.*870A>C) c.2278A>C (p.Met760Leu) c.337A>C c.2269A>C (p.Met757Leu) c.2260A>C (p.Met754Leu) c.2170A>C (p.Met724Leu) n.2731A>C n.321A>C | dbSNP |
| 1 | g.156881529A>G | CA342941575 | NTRK1 | c.2098A>G (p.Met700Val) c.*870A>G (n.*870A>G) c.2278A>G (p.Met760Val) c.337A>G c.2269A>G (p.Met757Val) c.2260A>G (p.Met754Val) c.2170A>G (p.Met724Val) n.2731A>G n.321A>G | |
| 1 | g.156881529A>T | CA342941576 | NTRK1 | c.2098A>T (p.Met700Leu) c.*870A>T (n.*870A>T) c.2278A>T (p.Met760Leu) c.337A>T c.2269A>T (p.Met757Leu) c.2260A>T (p.Met754Leu) c.2170A>T (p.Met724Leu) n.2731A>T n.321A>T | dbSNP |
| 1 | g.156881530T>A | CA342941578 | NTRK1 | c.2099T>A (p.Met700Lys) c.*871T>A (n.*871T>A) c.2279T>A (p.Met760Lys) c.338T>A c.2270T>A (p.Met757Lys) c.2261T>A (p.Met754Lys) c.2171T>A (p.Met724Lys) n.2732T>A n.322T>A | dbSNP gnomAD v4 |
| 1 | g.156881530T>C | CA342941579 | NTRK1 | c.2099T>C (p.Met700Thr) c.*871T>C (n.*871T>C) c.2279T>C (p.Met760Thr) c.338T>C c.2270T>C (p.Met757Thr) c.2261T>C (p.Met754Thr) c.2171T>C (p.Met724Thr) n.2732T>C n.322T>C | dbSNP |
| 1 | g.156881530T>G | CA342941580 | NTRK1 | c.2099T>G (p.Met700Arg) c.*871T>G (n.*871T>G) c.2279T>G (p.Met760Arg) c.338T>G c.2270T>G (p.Met757Arg) c.2261T>G (p.Met754Arg) c.2171T>G (p.Met724Arg) n.2732T>G n.322T>G | dbSNP gnomAD v4 |
| 1 | g.156881531G>A | CA342941582 | NTRK1 | c.2100G>A (p.Met700Ile) c.*872G>A (n.*872G>A) c.2280G>A (p.Met760Ile) c.339G>A c.2271G>A (p.Met757Ile) c.2262G>A (p.Met754Ile) c.2172G>A (p.Met724Ile) n.2733G>A n.323G>A | |
| 1 | g.156881531G>C | CA342941584 | NTRK1 | c.2100G>C (p.Met700Ile) c.*872G>C (n.*872G>C) c.2280G>C (p.Met760Ile) c.339G>C c.2271G>C (p.Met757Ile) c.2262G>C (p.Met754Ile) c.2172G>C (p.Met724Ile) n.2733G>C n.323G>C | gnomAD v4 |
| 1 | g.156881531G>T | CA342941583 | NTRK1 | c.2100G>T (p.Met700Ile) c.*872G>T (n.*872G>T) c.2280G>T (p.Met760Ile) c.339G>T c.2271G>T (p.Met757Ile) c.2262G>T (p.Met754Ile) c.2172G>T (p.Met724Ile) n.2733G>T n.323G>T | gnomAD v4 |
| 1 | g.156881532C>A | CA421140639 | NTRK1 | c.2101C>A (p.Arg701=) c.*873C>A (n.*873C>A) c.2281C>A (p.Arg761=) c.340C>A c.2272C>A (p.Arg758=) c.2263C>A (p.Arg755=) c.2173C>A (p.Arg725=) n.2734C>A n.324C>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156881532C= | CA1200788784 | NTRK1 | c.2101C= (p.Arg701=) c.*873C= (n.*873C=) c.2281C= (p.Arg761=) c.340C= c.2272C= (p.Arg758=) c.2263C= (p.Arg755=) c.2173C= (p.Arg725=) n.2734C= n.324C= | |
| 1 | g.156881532C>G | CA342941585 | NTRK1 | c.2101C>G (p.Arg701Gly) c.*873C>G (n.*873C>G) c.2281C>G (p.Arg761Gly) c.340C>G c.2272C>G (p.Arg758Gly) c.2263C>G (p.Arg755Gly) c.2173C>G (p.Arg725Gly) n.2734C>G n.324C>G | |
| 1 | g.156881532C>T | CA1169622 | NTRK1 | c.2101C>T (p.Arg701Trp) c.*873C>T (n.*873C>T) c.2281C>T (p.Arg761Trp) c.340C>T c.2272C>T (p.Arg758Trp) c.2263C>T (p.Arg755Trp) c.2173C>T (p.Arg725Trp) n.2734C>T n.324C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.156881533G>A | CA1169623 | NTRK1 | c.2102G>A (p.Arg701Gln) c.*874G>A (n.*874G>A) c.2282G>A (p.Arg761Gln) c.341G>A c.2273G>A (p.Arg758Gln) c.2264G>A (p.Arg755Gln) c.2174G>A (p.Arg725Gln) n.2735G>A n.325G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881533G>C | CA342941588 | NTRK1 | c.2102G>C (p.Arg701Pro) c.*874G>C (n.*874G>C) c.2282G>C (p.Arg761Pro) c.341G>C c.2273G>C (p.Arg758Pro) c.2264G>C (p.Arg755Pro) c.2174G>C (p.Arg725Pro) n.2735G>C n.325G>C | dbSNP gnomAD v4 |
| 1 | g.156881533G= | CA1143512578 | NTRK1 | c.2102G= (p.Arg701=) c.*874G= (n.*874G=) c.2282G= (p.Arg761=) c.341G= c.2273G= (p.Arg758=) c.2264G= (p.Arg755=) c.2174G= (p.Arg725=) n.2735G= n.325G= | |
| 1 | g.156881533G>T | CA342941589 | NTRK1 | c.2102G>T (p.Arg701Leu) c.*874G>T (n.*874G>T) c.2282G>T (p.Arg761Leu) c.341G>T c.2273G>T (p.Arg758Leu) c.2264G>T (p.Arg755Leu) c.2174G>T (p.Arg725Leu) n.2735G>T n.325G>T | gnomAD v4 |
| 1 | g.156881536del | CA2573926854 | NTRK1 | c.2105del (p.Gly702AlafsTer?) c.*877del (n.*877del) c.2285del (p.Gly762AlafsTer?) c.344del c.2276del (p.Gly759AlafsTer?) c.2267del (p.Gly756AlafsTer?) c.2177del (p.Gly726AlafsTer?) n.2738del n.328del | |
| 1 | g.156881534G>A | CA421140640 | NTRK1 | c.2103G>A (p.Arg701=) c.*875G>A (n.*875G>A) c.2283G>A (p.Arg761=) c.342G>A c.2274G>A (p.Arg758=) c.2265G>A (p.Arg755=) c.2175G>A (p.Arg725=) n.2736G>A n.326G>A | dbSNP |
| 1 | g.156881534G>C | CA421140641 | NTRK1 | c.2103G>C (p.Arg701=) c.*875G>C (n.*875G>C) c.2283G>C (p.Arg761=) c.342G>C c.2274G>C (p.Arg758=) c.2265G>C (p.Arg755=) c.2175G>C (p.Arg725=) n.2736G>C n.326G>C | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881534G= | CA1200788794 | NTRK1 | c.2103G= (p.Arg701=) c.*875G= (n.*875G=) c.2283G= (p.Arg761=) c.342G= c.2274G= (p.Arg758=) c.2265G= (p.Arg755=) c.2175G= (p.Arg725=) n.2736G= n.326G= | |
| 1 | g.156881534G>T | CA421140642 | NTRK1 | c.2103G>T (p.Arg701=) c.*875G>T (n.*875G>T) c.2283G>T (p.Arg761=) c.342G>T c.2274G>T (p.Arg758=) c.2265G>T (p.Arg755=) c.2175G>T (p.Arg725=) n.2736G>T n.326G>T | |
| 1 | g.156881535G>A | CA342941590 | NTRK1 | c.2104G>A (p.Gly702Ser) c.*876G>A (n.*876G>A) c.2284G>A (p.Gly762Ser) c.343G>A c.2275G>A (p.Gly759Ser) c.2266G>A (p.Gly756Ser) c.2176G>A (p.Gly726Ser) n.2737G>A n.327G>A | dbSNP gnomAD v2 |
| 1 | g.156881535G>C | CA1169624 | NTRK1 | c.2104G>C (p.Gly702Arg) c.*876G>C (n.*876G>C) c.2284G>C (p.Gly762Arg) c.343G>C c.2275G>C (p.Gly759Arg) c.2266G>C (p.Gly756Arg) c.2176G>C (p.Gly726Arg) n.2737G>C n.327G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881535G= | CA1200788796 | NTRK1 | c.2104G= (p.Gly702=) c.*876G= (n.*876G=) c.2284G= (p.Gly762=) c.343G= c.2275G= (p.Gly759=) c.2266G= (p.Gly756=) c.2176G= (p.Gly726=) n.2737G= n.327G= | |
| 1 | g.156881535G>T | CA342941592 | NTRK1 | c.2104G>T (p.Gly702Cys) c.*876G>T (n.*876G>T) c.2284G>T (p.Gly762Cys) c.343G>T c.2275G>T (p.Gly759Cys) c.2266G>T (p.Gly756Cys) c.2176G>T (p.Gly726Cys) n.2737G>T n.327G>T | gnomAD v4 |
| 1 | g.156881536G>A | CA342941594 | NTRK1 | c.2105G>A (p.Gly702Asp) c.*877G>A (n.*877G>A) c.2285G>A (p.Gly762Asp) c.344G>A c.2276G>A (p.Gly759Asp) c.2267G>A (p.Gly756Asp) c.2177G>A (p.Gly726Asp) n.2738G>A n.328G>A | dbSNP gnomAD v4 |
| 1 | g.156881536G>C | CA342941596 | NTRK1 | c.2105G>C (p.Gly702Ala) c.*877G>C (n.*877G>C) c.2285G>C (p.Gly762Ala) c.344G>C c.2276G>C (p.Gly759Ala) c.2267G>C (p.Gly756Ala) c.2177G>C (p.Gly726Ala) n.2738G>C n.328G>C | dbSNP |
| 1 | g.156881536G>T | CA342941597 | NTRK1 | c.2105G>T (p.Gly702Val) c.*877G>T (n.*877G>T) c.2285G>T (p.Gly762Val) c.344G>T c.2276G>T (p.Gly759Val) c.2267G>T (p.Gly756Val) c.2177G>T (p.Gly726Val) n.2738G>T n.328G>T | gnomAD v4 |
| 1 | g.156881537C>A | CA421140645 | NTRK1 | c.2106C>A (p.Gly702=) c.*878C>A (n.*878C>A) c.2286C>A (p.Gly762=) c.345C>A c.2277C>A (p.Gly759=) c.2268C>A (p.Gly756=) c.2178C>A (p.Gly726=) n.2739C>A n.329C>A | dbSNP gnomAD v4 |
| 1 | g.156881537C>G | CA421140643 | NTRK1 | c.2106C>G (p.Gly702=) c.*878C>G (n.*878C>G) c.2286C>G (p.Gly762=) c.345C>G c.2277C>G (p.Gly759=) c.2268C>G (p.Gly756=) c.2178C>G (p.Gly726=) n.2739C>G n.329C>G | dbSNP |
| 1 | g.156881537C>T | CA421140644 | NTRK1 | c.2106C>T (p.Gly702=) c.*878C>T (n.*878C>T) c.2286C>T (p.Gly762=) c.345C>T c.2277C>T (p.Gly759=) c.2268C>T (p.Gly756=) c.2178C>T (p.Gly726=) n.2739C>T n.329C>T | dbSNP |
| 1 | g.156881538T>A | CA342941600 | NTRK1 | c.2107T>A (p.Cys703Ser) c.*879T>A (n.*879T>A) c.2287T>A (p.Cys763Ser) c.346T>A c.2278T>A (p.Cys760Ser) c.2269T>A (p.Cys757Ser) c.2179T>A (p.Cys727Ser) n.2740T>A n.330T>A | dbSNP |
| 1 | g.156881538T>C | CA342941599 | NTRK1 | c.2107T>C (p.Cys703Arg) c.*879T>C (n.*879T>C) c.2287T>C (p.Cys763Arg) c.346T>C c.2278T>C (p.Cys760Arg) c.2269T>C (p.Cys757Arg) c.2179T>C (p.Cys727Arg) n.2740T>C n.330T>C | |
| 1 | g.156881538T>G | CA342941598 | NTRK1 | c.2107T>G (p.Cys703Gly) c.*879T>G (n.*879T>G) c.2287T>G (p.Cys763Gly) c.346T>G c.2278T>G (p.Cys760Gly) c.2269T>G (p.Cys757Gly) c.2179T>G (p.Cys727Gly) n.2740T>G n.330T>G | |
| 1 | g.156881539G>A | CA342941605 | NTRK1 | c.2108G>A (p.Cys703Tyr) c.*880G>A (n.*880G>A) c.2288G>A (p.Cys763Tyr) c.347G>A c.2279G>A (p.Cys760Tyr) c.2270G>A (p.Cys757Tyr) c.2180G>A (p.Cys727Tyr) n.2741G>A n.331G>A | gnomAD v4 |
| 1 | g.156881539G>C | CA342941601 | NTRK1 | c.2108G>C (p.Cys703Ser) c.*880G>C (n.*880G>C) c.2288G>C (p.Cys763Ser) c.347G>C c.2279G>C (p.Cys760Ser) c.2270G>C (p.Cys757Ser) c.2180G>C (p.Cys727Ser) n.2741G>C n.331G>C | gnomAD v4 |
| 1 | g.156881539G>T | CA342941603 | NTRK1 | c.2108G>T (p.Cys703Phe) c.*880G>T (n.*880G>T) c.2288G>T (p.Cys763Phe) c.347G>T c.2279G>T (p.Cys760Phe) c.2270G>T (p.Cys757Phe) c.2180G>T (p.Cys727Phe) n.2741G>T n.331G>T | gnomAD v4 |
| 1 | g.156881540C>A | CA342941606 | NTRK1 | c.2109C>A (p.Cys703Ter) c.*881C>A (n.*881C>A) c.2289C>A (p.Cys763Ter) c.348C>A c.2280C>A (p.Cys760Ter) c.2271C>A (p.Cys757Ter) c.2181C>A (p.Cys727Ter) n.2742C>A n.332C>A | gnomAD v4 |
| 1 | g.156881540C= | CA1200788799 | NTRK1 | c.2109C= (p.Cys703=) c.*881C= (n.*881C=) c.2289C= (p.Cys763=) c.348C= c.2280C= (p.Cys760=) c.2271C= (p.Cys757=) c.2181C= (p.Cys727=) n.2742C= n.332C= | |
| 1 | g.156881540C>G | CA342941607 | NTRK1 | c.2109C>G (p.Cys703Trp) c.*881C>G (n.*881C>G) c.2289C>G (p.Cys763Trp) c.348C>G c.2280C>G (p.Cys760Trp) c.2271C>G (p.Cys757Trp) c.2181C>G (p.Cys727Trp) n.2742C>G n.332C>G | ClinVar dbSNP |
| 1 | g.156881540C>T | CA421140646 | NTRK1 | c.2109C>T (p.Cys703=) c.*881C>T (n.*881C>T) c.2289C>T (p.Cys763=) c.348C>T c.2280C>T (p.Cys760=) c.2271C>T (p.Cys757=) c.2181C>T (p.Cys727=) n.2742C>T n.332C>T | dbSNP gnomAD v4 |
| 1 | g.156881541T>A | CA342941609 | NTRK1 | c.2110T>A (p.Trp704Arg) c.*882T>A (n.*882T>A) c.2290T>A (p.Trp764Arg) c.349T>A c.2281T>A (p.Trp761Arg) c.2272T>A (p.Trp758Arg) c.2182T>A (p.Trp728Arg) n.2743T>A n.333T>A | |
| 1 | g.156881541T>C | CA342941612 | NTRK1 | c.2110T>C (p.Trp704Arg) c.*882T>C (n.*882T>C) c.2290T>C (p.Trp764Arg) c.349T>C c.2281T>C (p.Trp761Arg) c.2272T>C (p.Trp758Arg) c.2182T>C (p.Trp728Arg) n.2743T>C n.333T>C | gnomAD v4 |
| 1 | g.156881541T>G | CA342941613 | NTRK1 | c.2110T>G (p.Trp704Gly) c.*882T>G (n.*882T>G) c.2290T>G (p.Trp764Gly) c.349T>G c.2281T>G (p.Trp761Gly) c.2272T>G (p.Trp758Gly) c.2182T>G (p.Trp728Gly) n.2743T>G n.333T>G | |
| 1 | g.156881542G>A | CA342941615 | NTRK1 | c.2111G>A (p.Trp704Ter) c.*883G>A (n.*883G>A) c.2291G>A (p.Trp764Ter) c.350G>A c.2282G>A (p.Trp761Ter) c.2273G>A (p.Trp758Ter) c.2183G>A (p.Trp728Ter) n.2744G>A n.334G>A | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881542G>C | CA342941616 | NTRK1 | c.2111G>C (p.Trp704Ser) c.*883G>C (n.*883G>C) c.2291G>C (p.Trp764Ser) c.350G>C c.2282G>C (p.Trp761Ser) c.2273G>C (p.Trp758Ser) c.2183G>C (p.Trp728Ser) n.2744G>C n.334G>C | dbSNP |
| 1 | g.156881542G= | CA1200788802 | NTRK1 | c.2111G= (p.Trp704=) c.*883G= (n.*883G=) c.2291G= (p.Trp764=) c.350G= c.2282G= (p.Trp761=) c.2273G= (p.Trp758=) c.2183G= (p.Trp728=) n.2744G= n.334G= | |
| 1 | g.156881542G>T | CA342941617 | NTRK1 | c.2111G>T (p.Trp704Leu) c.*883G>T (n.*883G>T) c.2291G>T (p.Trp764Leu) c.350G>T c.2282G>T (p.Trp761Leu) c.2273G>T (p.Trp758Leu) c.2183G>T (p.Trp728Leu) n.2744G>T n.334G>T | |
| 1 | g.156881543G>A | CA342941619 | NTRK1 | c.2112G>A (p.Trp704Ter) c.*884G>A (n.*884G>A) c.2292G>A (p.Trp764Ter) c.351G>A c.2283G>A (p.Trp761Ter) c.2274G>A (p.Trp758Ter) c.2184G>A (p.Trp728Ter) n.2745G>A n.335G>A | dbSNP gnomAD v4 |
| 1 | g.156881543G>C | CA342941620 | NTRK1 | c.2112G>C (p.Trp704Cys) c.*884G>C (n.*884G>C) c.2292G>C (p.Trp764Cys) c.351G>C c.2283G>C (p.Trp761Cys) c.2274G>C (p.Trp758Cys) c.2184G>C (p.Trp728Cys) n.2745G>C n.335G>C | dbSNP |
| 1 | g.156881543G= | CA1200788806 | NTRK1 | c.2112G= (p.Trp704=) c.*884G= (n.*884G=) c.2292G= (p.Trp764=) c.351G= c.2283G= (p.Trp761=) c.2274G= (p.Trp758=) c.2184G= (p.Trp728=) n.2745G= n.335G= | |
| 1 | g.156881543G>T | CA342941621 | NTRK1 | c.2112G>T (p.Trp704Cys) c.*884G>T (n.*884G>T) c.2292G>T (p.Trp764Cys) c.351G>T c.2283G>T (p.Trp761Cys) c.2274G>T (p.Trp758Cys) c.2184G>T (p.Trp728Cys) n.2745G>T n.335G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881544C>A | CA342941624 | NTRK1 | c.2113C>A (p.Gln705Lys) c.*885C>A (n.*885C>A) c.2293C>A (p.Gln765Lys) c.352C>A c.2284C>A (p.Gln762Lys) c.2275C>A (p.Gln759Lys) c.2185C>A (p.Gln729Lys) n.2746C>A n.336C>A | gnomAD v4 |
| 1 | g.156881544C>G | CA342941622 | NTRK1 | c.2113C>G (p.Gln705Glu) c.*885C>G (n.*885C>G) c.2293C>G (p.Gln765Glu) c.352C>G c.2284C>G (p.Gln762Glu) c.2275C>G (p.Gln759Glu) c.2185C>G (p.Gln729Glu) n.2746C>G n.336C>G | dbSNP |
| 1 | g.156881544C>T | CA342941623 | NTRK1 | c.2113C>T (p.Gln705Ter) c.*885C>T (n.*885C>T) c.2293C>T (p.Gln765Ter) c.352C>T c.2284C>T (p.Gln762Ter) c.2275C>T (p.Gln759Ter) c.2185C>T (p.Gln729Ter) n.2746C>T n.336C>T | dbSNP gnomAD v4 |
| 1 | g.156881545A>C | CA342941625 | NTRK1 | c.2114A>C (p.Gln705Pro) c.*886A>C (n.*886A>C) c.2294A>C (p.Gln765Pro) c.353A>C c.2285A>C (p.Gln762Pro) c.2276A>C (p.Gln759Pro) c.2186A>C (p.Gln729Pro) n.2747A>C n.337A>C | gnomAD v4 |
| 1 | g.156881545A>G | CA342941627 | NTRK1 | c.2114A>G (p.Gln705Arg) c.*886A>G (n.*886A>G) c.2294A>G (p.Gln765Arg) c.353A>G c.2285A>G (p.Gln762Arg) c.2276A>G (p.Gln759Arg) c.2186A>G (p.Gln729Arg) n.2747A>G n.337A>G | dbSNP |
| 1 | g.156881545A>T | CA342941628 | NTRK1 | c.2114A>T (p.Gln705Leu) c.*886A>T (n.*886A>T) c.2294A>T (p.Gln765Leu) c.353A>T c.2285A>T (p.Gln762Leu) c.2276A>T (p.Gln759Leu) c.2186A>T (p.Gln729Leu) n.2747A>T n.337A>T | dbSNP |
| 1 | g.156881546G>A | CA421140647 | NTRK1 | c.2115G>A (p.Gln705=) c.*887G>A (n.*887G>A) c.2295G>A (p.Gln765=) c.354G>A c.2286G>A (p.Gln762=) c.2277G>A (p.Gln759=) c.2187G>A (p.Gln729=) n.2748G>A n.338G>A | dbSNP COSMIC COSMIC |
| 1 | g.156881546G>C | CA342941629 | NTRK1 | c.2115G>C (p.Gln705His) c.*887G>C (n.*887G>C) c.2295G>C (p.Gln765His) c.354G>C c.2286G>C (p.Gln762His) c.2277G>C (p.Gln759His) c.2187G>C (p.Gln729His) n.2748G>C n.338G>C | dbSNP |
| 1 | g.156881546G>T | CA342941630 | NTRK1 | c.2115G>T (p.Gln705His) c.*887G>T (n.*887G>T) c.2295G>T (p.Gln765His) c.354G>T c.2286G>T (p.Gln762His) c.2277G>T (p.Gln759His) c.2187G>T (p.Gln729His) n.2748G>T n.338G>T | gnomAD v4 |
| 1 | g.156881547C>A | CA421140648 | NTRK1 | c.2116C>A (p.Arg706=) c.*888C>A (n.*888C>A) c.2296C>A (p.Arg766=) c.355C>A c.2287C>A (p.Arg763=) c.2278C>A (p.Arg760=) c.2188C>A (p.Arg730=) n.2749C>A n.339C>A | |
| 1 | g.156881547C= | CA1200788811 | NTRK1 | c.2116C= (p.Arg706=) c.*888C= (n.*888C=) c.2296C= (p.Arg766=) c.355C= c.2287C= (p.Arg763=) c.2278C= (p.Arg760=) c.2188C= (p.Arg730=) n.2749C= n.339C= | |
| 1 | g.156881547C>G | CA342941631 | NTRK1 | c.2116C>G (p.Arg706Gly) c.*888C>G (n.*888C>G) c.2296C>G (p.Arg766Gly) c.355C>G c.2287C>G (p.Arg763Gly) c.2278C>G (p.Arg760Gly) c.2188C>G (p.Arg730Gly) n.2749C>G n.339C>G | |
| 1 | g.156881547C>T | CA1169625 | NTRK1 | c.2116C>T (p.Arg706Trp) c.*888C>T (n.*888C>T) c.2296C>T (p.Arg766Trp) c.355C>T c.2287C>T (p.Arg763Trp) c.2278C>T (p.Arg760Trp) c.2188C>T (p.Arg730Trp) n.2749C>T n.339C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881548G>A | CA1169626 | NTRK1 | c.2117G>A (p.Arg706Gln) c.*889G>A (n.*889G>A) c.2297G>A (p.Arg766Gln) c.356G>A c.2288G>A (p.Arg763Gln) c.2279G>A (p.Arg760Gln) c.2189G>A (p.Arg730Gln) n.2750G>A n.340G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881548G>C | CA342941633 | NTRK1 | c.2117G>C (p.Arg706Pro) c.*889G>C (n.*889G>C) c.2297G>C (p.Arg766Pro) c.356G>C c.2288G>C (p.Arg763Pro) c.2279G>C (p.Arg760Pro) c.2189G>C (p.Arg730Pro) n.2750G>C n.340G>C | dbSNP |
| 1 | g.156881548G= | CA1200788819 | NTRK1 | c.2117G= (p.Arg706=) c.*889G= (n.*889G=) c.2297G= (p.Arg766=) c.356G= c.2288G= (p.Arg763=) c.2279G= (p.Arg760=) c.2189G= (p.Arg730=) n.2750G= n.340G= | |
| 1 | g.156881548G>T | CA342941634 | NTRK1 | c.2117G>T (p.Arg706Leu) c.*889G>T (n.*889G>T) c.2297G>T (p.Arg766Leu) c.356G>T c.2288G>T (p.Arg763Leu) c.2279G>T (p.Arg760Leu) c.2189G>T (p.Arg730Leu) n.2750G>T n.340G>T | dbSNP gnomAD v2 COSMIC COSMIC |
| 1 | g.156881549G>A | CA421140649 | NTRK1 | c.2118G>A (p.Arg706=) c.*890G>A (n.*890G>A) c.2298G>A (p.Arg766=) c.357G>A c.2289G>A (p.Arg763=) c.2280G>A (p.Arg760=) c.2190G>A (p.Arg730=) n.2751G>A n.341G>A | dbSNP COSMIC COSMIC |
| 1 | g.156881549G>C | CA421140650 | NTRK1 | c.2118G>C (p.Arg706=) c.*890G>C (n.*890G>C) c.2298G>C (p.Arg766=) c.357G>C c.2289G>C (p.Arg763=) c.2280G>C (p.Arg760=) c.2190G>C (p.Arg730=) n.2751G>C n.341G>C | dbSNP |
| 1 | g.156881549G= | CA1200788827 | NTRK1 | c.2118G= (p.Arg706=) c.*890G= (n.*890G=) c.2298G= (p.Arg766=) c.357G= c.2289G= (p.Arg763=) c.2280G= (p.Arg760=) c.2190G= (p.Arg730=) n.2751G= n.341G= | |
| 1 | g.156881549G>T | CA421140651 | NTRK1 | c.2118G>T (p.Arg706=) c.*890G>T (n.*890G>T) c.2298G>T (p.Arg766=) c.357G>T c.2289G>T (p.Arg763=) c.2280G>T (p.Arg760=) c.2190G>T (p.Arg730=) n.2751G>T n.341G>T | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881550G>A | CA342941635 | NTRK1 | c.2119G>A (p.Glu707Lys) c.*891G>A (n.*891G>A) c.2299G>A (p.Glu767Lys) c.358G>A c.2290G>A (p.Glu764Lys) c.2281G>A (p.Glu761Lys) c.2191G>A (p.Glu731Lys) n.2752G>A n.342G>A | dbSNP gnomAD v4 |
| 1 | g.156881550G>C | CA10608362 | NTRK1 | c.2119G>C (p.Glu707Gln) c.*891G>C (n.*891G>C) c.2299G>C (p.Glu767Gln) c.358G>C c.2290G>C (p.Glu764Gln) c.2281G>C (p.Glu761Gln) c.2191G>C (p.Glu731Gln) n.2752G>C n.342G>C | ClinVar dbSNP |
| 1 | g.156881550G= | CA1200788831 | NTRK1 | c.2119G= (p.Glu707=) c.*891G= (n.*891G=) c.2299G= (p.Glu767=) c.358G= c.2290G= (p.Glu764=) c.2281G= (p.Glu761=) c.2191G= (p.Glu731=) n.2752G= n.342G= | |
| 1 | g.156881550G>T | CA342941636 | NTRK1 | c.2119G>T (p.Glu707Ter) c.*891G>T (n.*891G>T) c.2299G>T (p.Glu767Ter) c.358G>T c.2290G>T (p.Glu764Ter) c.2281G>T (p.Glu761Ter) c.2191G>T (p.Glu731Ter) n.2752G>T n.342G>T | |
| 1 | g.156881551A>C | CA342941638 | NTRK1 | c.2120A>C (p.Glu707Ala) c.*892A>C (n.*892A>C) c.2300A>C (p.Glu767Ala) c.359A>C c.2291A>C (p.Glu764Ala) c.2282A>C (p.Glu761Ala) c.2192A>C (p.Glu731Ala) n.2753A>C n.343A>C | |
| 1 | g.156881551A>G | CA342941639 | NTRK1 | c.2120A>G (p.Glu707Gly) c.*892A>G (n.*892A>G) c.2300A>G (p.Glu767Gly) c.359A>G c.2291A>G (p.Glu764Gly) c.2282A>G (p.Glu761Gly) c.2192A>G (p.Glu731Gly) n.2753A>G n.343A>G | dbSNP |
| 1 | g.156881551A>T | CA342941637 | NTRK1 | c.2120A>T (p.Glu707Val) c.*892A>T (n.*892A>T) c.2300A>T (p.Glu767Val) c.359A>T c.2291A>T (p.Glu764Val) c.2282A>T (p.Glu761Val) c.2192A>T (p.Glu731Val) n.2753A>T n.343A>T | dbSNP |
| 1 | g.156881552G>A | CA421140652 | NTRK1 | c.2121G>A (p.Glu707=) c.*893G>A (n.*893G>A) c.2301G>A (p.Glu767=) c.360G>A c.2292G>A (p.Glu764=) c.2283G>A (p.Glu761=) c.2193G>A (p.Glu731=) n.2754G>A n.344G>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156881552G>C | CA1169627 | NTRK1 | c.2121G>C (p.Glu707Asp) c.*893G>C (n.*893G>C) c.2301G>C (p.Glu767Asp) c.360G>C c.2292G>C (p.Glu764Asp) c.2283G>C (p.Glu761Asp) c.2193G>C (p.Glu731Asp) n.2754G>C n.344G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881552G= | CA1200788837 | NTRK1 | c.2121G= (p.Glu707=) c.*893G= (n.*893G=) c.2301G= (p.Glu767=) c.360G= c.2292G= (p.Glu764=) c.2283G= (p.Glu761=) c.2193G= (p.Glu731=) n.2754G= n.344G= | |
| 1 | g.156881552G>T | CA31126179 | NTRK1 | c.2121G>T (p.Glu707Asp) c.*893G>T (n.*893G>T) c.2301G>T (p.Glu767Asp) c.360G>T c.2292G>T (p.Glu764Asp) c.2283G>T (p.Glu761Asp) c.2193G>T (p.Glu731Asp) n.2754G>T n.344G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881553C>A | CA342941640 | NTRK1 | c.2122C>A (p.Pro708Thr) c.*894C>A (n.*894C>A) c.2302C>A (p.Pro768Thr) c.361C>A c.2293C>A (p.Pro765Thr) c.2284C>A (p.Pro762Thr) c.2194C>A (p.Pro732Thr) n.2755C>A n.345C>A | dbSNP gnomAD v4 |
| 1 | g.156881553C>G | CA342941641 | NTRK1 | c.2122C>G (p.Pro708Ala) c.*894C>G (n.*894C>G) c.2302C>G (p.Pro768Ala) c.361C>G c.2293C>G (p.Pro765Ala) c.2284C>G (p.Pro762Ala) c.2194C>G (p.Pro732Ala) n.2755C>G n.345C>G | dbSNP |
| 1 | g.156881553C>T | CA342941642 | NTRK1 | c.2122C>T (p.Pro708Ser) c.*894C>T (n.*894C>T) c.2302C>T (p.Pro768Ser) c.361C>T c.2293C>T (p.Pro765Ser) c.2284C>T (p.Pro762Ser) c.2194C>T (p.Pro732Ser) n.2755C>T n.345C>T | dbSNP gnomAD v4 COSMIC COSMIC |
| 1 | g.156881554C>A | CA342941643 | NTRK1 | c.2123C>A (p.Pro708His) c.*895C>A (n.*895C>A) c.2303C>A (p.Pro768His) c.362C>A c.2294C>A (p.Pro765His) c.2285C>A (p.Pro762His) c.2195C>A (p.Pro732His) n.2756C>A n.346C>A | dbSNP |
| 1 | g.156881554C= | CA1200788843 | NTRK1 | c.2123C= (p.Pro708=) c.*895C= (n.*895C=) c.2303C= (p.Pro768=) c.362C= c.2294C= (p.Pro765=) c.2285C= (p.Pro762=) c.2195C= (p.Pro732=) n.2756C= n.346C= | |
| 1 | g.156881554C>G | CA342941644 | NTRK1 | c.2123C>G (p.Pro708Arg) c.*895C>G (n.*895C>G) c.2303C>G (p.Pro768Arg) c.362C>G c.2294C>G (p.Pro765Arg) c.2285C>G (p.Pro762Arg) c.2195C>G (p.Pro732Arg) n.2756C>G n.346C>G | dbSNP |
| 1 | g.156881554C>T | CA1169628 | NTRK1 | c.2123C>T (p.Pro708Leu) c.*895C>T (n.*895C>T) c.2303C>T (p.Pro768Leu) c.362C>T c.2294C>T (p.Pro765Leu) c.2285C>T (p.Pro762Leu) c.2195C>T (p.Pro732Leu) n.2756C>T n.346C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881555C>A | CA421140653 | NTRK1 | c.2124C>A (p.Pro708=) c.*896C>A (n.*896C>A) c.2304C>A (p.Pro768=) c.363C>A c.2295C>A (p.Pro765=) c.2286C>A (p.Pro762=) c.2196C>A (p.Pro732=) n.2757C>A n.347C>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156881555C>G | CA421140654 | NTRK1 | c.2124C>G (p.Pro708=) c.*896C>G (n.*896C>G) c.2304C>G (p.Pro768=) c.363C>G c.2295C>G (p.Pro765=) c.2286C>G (p.Pro762=) c.2196C>G (p.Pro732=) n.2757C>G n.347C>G | dbSNP |
| 1 | g.156881555C>T | CA421140655 | NTRK1 | c.2124C>T (p.Pro708=) c.*896C>T (n.*896C>T) c.2304C>T (p.Pro768=) c.363C>T c.2295C>T (p.Pro765=) c.2286C>T (p.Pro762=) c.2196C>T (p.Pro732=) n.2757C>T n.347C>T | dbSNP gnomAD v4 |
| 1 | g.156881556C>A | CA342941645 | NTRK1 | c.2125C>A (p.Gln709Lys) c.*897C>A (n.*897C>A) c.2305C>A (p.Gln769Lys) c.364C>A c.2296C>A (p.Gln766Lys) c.2287C>A (p.Gln763Lys) c.2197C>A (p.Gln733Lys) n.2758C>A n.348C>A | |
| 1 | g.156881556C>G | CA342941646 | NTRK1 | c.2125C>G (p.Gln709Glu) c.*897C>G (n.*897C>G) c.2305C>G (p.Gln769Glu) c.364C>G c.2296C>G (p.Gln766Glu) c.2287C>G (p.Gln763Glu) c.2197C>G (p.Gln733Glu) n.2758C>G n.348C>G | |
| 1 | g.156881556C>T | CA342941647 | NTRK1 | c.2125C>T (p.Gln709Ter) c.*897C>T (n.*897C>T) c.2305C>T (p.Gln769Ter) c.364C>T c.2296C>T (p.Gln766Ter) c.2287C>T (p.Gln763Ter) c.2197C>T (p.Gln733Ter) n.2758C>T n.348C>T | |
| 1 | g.156881557A>C | CA342941648 | NTRK1 | c.2126A>C (p.Gln709Pro) c.*898A>C (n.*898A>C) c.2306A>C (p.Gln769Pro) c.365A>C c.2297A>C (p.Gln766Pro) c.2288A>C (p.Gln763Pro) c.2198A>C (p.Gln733Pro) n.2759A>C n.349A>C | dbSNP |
| 1 | g.156881557A>G | CA342941650 | NTRK1 | c.2126A>G (p.Gln709Arg) c.*898A>G (n.*898A>G) c.2306A>G (p.Gln769Arg) c.365A>G c.2297A>G (p.Gln766Arg) c.2288A>G (p.Gln763Arg) c.2198A>G (p.Gln733Arg) n.2759A>G n.349A>G | dbSNP |
| 1 | g.156881557A>T | CA342941651 | NTRK1 | c.2126A>T (p.Gln709Leu) c.*898A>T (n.*898A>T) c.2306A>T (p.Gln769Leu) c.365A>T c.2297A>T (p.Gln766Leu) c.2288A>T (p.Gln763Leu) c.2198A>T (p.Gln733Leu) n.2759A>T n.349A>T | dbSNP |
| 1 | g.156881558G>A | CA421140656 | NTRK1 | c.2127G>A (p.Gln709=) c.*899G>A (n.*899G>A) c.2307G>A (p.Gln769=) c.366G>A c.2298G>A (p.Gln766=) c.2289G>A (p.Gln763=) c.2199G>A (p.Gln733=) n.2760G>A n.350G>A | dbSNP |
| 1 | g.156881558G>C | CA342941653 | NTRK1 | c.2127G>C (p.Gln709His) c.*899G>C (n.*899G>C) c.2307G>C (p.Gln769His) c.366G>C c.2298G>C (p.Gln766His) c.2289G>C (p.Gln763His) c.2199G>C (p.Gln733His) n.2760G>C n.350G>C | dbSNP |
| 1 | g.156881558G>T | CA342941652 | NTRK1 | c.2127G>T (p.Gln709His) c.*899G>T (n.*899G>T) c.2307G>T (p.Gln769His) c.366G>T c.2298G>T (p.Gln766His) c.2289G>T (p.Gln763His) c.2199G>T (p.Gln733His) n.2760G>T n.350G>T | |
| 1 | g.156881559C>A | CA342941654 | NTRK1 | c.2128C>A (p.Gln710Lys) c.*900C>A (n.*900C>A) c.2308C>A (p.Gln770Lys) c.367C>A c.2299C>A (p.Gln767Lys) c.2290C>A (p.Gln764Lys) c.2200C>A (p.Gln734Lys) n.2761C>A n.351C>A | ClinVar dbSNP |
| 1 | g.156881559C= | CA1200788849 | NTRK1 | c.2128C= (p.Gln710=) c.*900C= (n.*900C=) c.2308C= (p.Gln770=) c.367C= c.2299C= (p.Gln767=) c.2290C= (p.Gln764=) c.2200C= (p.Gln734=) n.2761C= n.351C= | |
| 1 | g.156881559C>G | CA342941655 | NTRK1 | c.2128C>G (p.Gln710Glu) c.*900C>G (n.*900C>G) c.2308C>G (p.Gln770Glu) c.367C>G c.2299C>G (p.Gln767Glu) c.2290C>G (p.Gln764Glu) c.2200C>G (p.Gln734Glu) n.2761C>G n.351C>G | dbSNP |
| 1 | g.156881559C>T | CA1169629 | NTRK1 | c.2128C>T (p.Gln710Ter) c.*900C>T (n.*900C>T) c.2308C>T (p.Gln770Ter) c.367C>T c.2299C>T (p.Gln767Ter) c.2290C>T (p.Gln764Ter) c.2200C>T (p.Gln734Ter) n.2761C>T n.351C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881560A>C | CA342941656 | NTRK1 | c.2129A>C (p.Gln710Pro) c.*901A>C (n.*901A>C) c.2309A>C (p.Gln770Pro) c.368A>C c.2300A>C (p.Gln767Pro) c.2291A>C (p.Gln764Pro) c.2201A>C (p.Gln734Pro) n.2762A>C n.352A>C | dbSNP |
| 1 | g.156881560A>G | CA342941658 | NTRK1 | c.2129A>G (p.Gln710Arg) c.*901A>G (n.*901A>G) c.2309A>G (p.Gln770Arg) c.368A>G c.2300A>G (p.Gln767Arg) c.2291A>G (p.Gln764Arg) c.2201A>G (p.Gln734Arg) n.2762A>G n.352A>G | dbSNP gnomAD v4 |
| 1 | g.156881560A>T | CA342941659 | NTRK1 | c.2129A>T (p.Gln710Leu) c.*901A>T (n.*901A>T) c.2309A>T (p.Gln770Leu) c.368A>T c.2300A>T (p.Gln767Leu) c.2291A>T (p.Gln764Leu) c.2201A>T (p.Gln734Leu) n.2762A>T n.352A>T | dbSNP |
| 1 | g.156881561A>C | CA342941662 | NTRK1 | c.2130A>C (p.Gln710His) c.*902A>C (n.*902A>C) c.2310A>C (p.Gln770His) c.369A>C c.2301A>C (p.Gln767His) c.2292A>C (p.Gln764His) c.2202A>C (p.Gln734His) n.2763A>C n.353A>C | dbSNP |
| 1 | g.156881561A>G | CA421140657 | NTRK1 | c.2130A>G (p.Gln710=) c.*902A>G (n.*902A>G) c.2310A>G (p.Gln770=) c.369A>G c.2301A>G (p.Gln767=) c.2292A>G (p.Gln764=) c.2202A>G (p.Gln734=) n.2763A>G n.353A>G | dbSNP gnomAD v4 |
| 1 | g.156881561A>T | CA342941660 | NTRK1 | c.2130A>T (p.Gln710His) c.*902A>T (n.*902A>T) c.2310A>T (p.Gln770His) c.369A>T c.2301A>T (p.Gln767His) c.2292A>T (p.Gln764His) c.2202A>T (p.Gln734His) n.2763A>T n.353A>T | dbSNP |
| 1 | g.156881562C>A | CA342941663 | NTRK1 | c.2131C>A (p.Arg711Ser) c.*903C>A (n.*903C>A) c.2311C>A (p.Arg771Ser) c.370C>A c.2302C>A (p.Arg768Ser) c.2293C>A (p.Arg765Ser) c.2203C>A (p.Arg735Ser) n.2764C>A n.354C>A | dbSNP gnomAD v4 |
| 1 | g.156881562C= | CA1200788853 | NTRK1 | c.2131C= (p.Arg711=) c.*903C= (n.*903C=) c.2311C= (p.Arg771=) c.370C= c.2302C= (p.Arg768=) c.2293C= (p.Arg765=) c.2203C= (p.Arg735=) n.2764C= n.354C= | |
| 1 | g.156881562C>G | CA342941664 | NTRK1 | c.2131C>G (p.Arg711Gly) c.*903C>G (n.*903C>G) c.2311C>G (p.Arg771Gly) c.370C>G c.2302C>G (p.Arg768Gly) c.2293C>G (p.Arg765Gly) c.2203C>G (p.Arg735Gly) n.2764C>G n.354C>G | dbSNP |
| 1 | g.156881562C>T | CA342941665 | NTRK1 | c.2131C>T (p.Arg711Cys) c.*903C>T (n.*903C>T) c.2311C>T (p.Arg771Cys) c.370C>T c.2302C>T (p.Arg768Cys) c.2293C>T (p.Arg765Cys) c.2203C>T (p.Arg735Cys) n.2764C>T n.354C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881563G>A | CA1169630 | NTRK1 | c.2132G>A (p.Arg711His) c.*904G>A (n.*904G>A) c.2312G>A (p.Arg771His) c.371G>A c.2303G>A (p.Arg768His) c.2294G>A (p.Arg765His) c.2204G>A (p.Arg735His) n.2765G>A n.355G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881563G>C | CA342941666 | NTRK1 | c.2132G>C (p.Arg711Pro) c.*904G>C (n.*904G>C) c.2312G>C (p.Arg771Pro) c.371G>C c.2303G>C (p.Arg768Pro) c.2294G>C (p.Arg765Pro) c.2204G>C (p.Arg735Pro) n.2765G>C n.355G>C | |
| 1 | g.156881563G= | CA1200788861 | NTRK1 | c.2132G= (p.Arg711=) c.*904G= (n.*904G=) c.2312G= (p.Arg771=) c.371G= c.2303G= (p.Arg768=) c.2294G= (p.Arg765=) c.2204G= (p.Arg735=) n.2765G= n.355G= | |
| 1 | g.156881563G>T | CA342941667 | NTRK1 | c.2132G>T (p.Arg711Leu) c.*904G>T (n.*904G>T) c.2312G>T (p.Arg771Leu) c.371G>T c.2303G>T (p.Arg768Leu) c.2294G>T (p.Arg765Leu) c.2204G>T (p.Arg735Leu) n.2765G>T n.355G>T | |
| 1 | g.156881564C>A | CA421140658 | NTRK1 | c.2133C>A (p.Arg711=) c.*905C>A (n.*905C>A) c.2313C>A (p.Arg771=) c.372C>A c.2304C>A (p.Arg768=) c.2295C>A (p.Arg765=) c.2205C>A (p.Arg735=) n.2766C>A n.356C>A | ClinVar dbSNP |
| 1 | g.156881564C>G | CA421140659 | NTRK1 | c.2133C>G (p.Arg711=) c.*905C>G (n.*905C>G) c.2313C>G (p.Arg771=) c.372C>G c.2304C>G (p.Arg768=) c.2295C>G (p.Arg765=) c.2205C>G (p.Arg735=) n.2766C>G n.356C>G | dbSNP |
| 1 | g.156881564C>T | CA421140660 | NTRK1 | c.2133C>T (p.Arg711=) c.*905C>T (n.*905C>T) c.2313C>T (p.Arg771=) c.372C>T c.2304C>T (p.Arg768=) c.2295C>T (p.Arg765=) c.2205C>T (p.Arg735=) n.2766C>T n.356C>T | ClinVar dbSNP |
| 1 | g.156881565C>A | CA342941668 | NTRK1 | c.2134C>A (p.His712Asn) c.*906C>A (n.*906C>A) c.2314C>A (p.His772Asn) c.373C>A c.2305C>A (p.His769Asn) c.2296C>A (p.His766Asn) c.2206C>A (p.His736Asn) n.2767C>A n.357C>A | |
| 1 | g.156881565C>G | CA342941671 | NTRK1 | c.2134C>G (p.His712Asp) c.*906C>G (n.*906C>G) c.2314C>G (p.His772Asp) c.373C>G c.2305C>G (p.His769Asp) c.2296C>G (p.His766Asp) c.2206C>G (p.His736Asp) n.2767C>G n.357C>G | dbSNP |
| 1 | g.156881565C>T | CA342941669 | NTRK1 | c.2134C>T (p.His712Tyr) c.*906C>T (n.*906C>T) c.2314C>T (p.His772Tyr) c.373C>T c.2305C>T (p.His769Tyr) c.2296C>T (p.His766Tyr) c.2206C>T (p.His736Tyr) n.2767C>T n.357C>T | dbSNP |
| 1 | g.156881566A= | CA1200788866 | NTRK1 | c.2135A= (p.His712=) c.*907A= (n.*907A=) c.2315A= (p.His772=) c.374A= c.2306A= (p.His769=) c.2297A= (p.His766=) c.2207A= (p.His736=) n.2768A= n.358A= | |
| 1 | g.156881566A>C | CA342941672 | NTRK1 | c.2135A>C (p.His712Pro) c.*907A>C (n.*907A>C) c.2315A>C (p.His772Pro) c.374A>C c.2306A>C (p.His769Pro) c.2297A>C (p.His766Pro) c.2207A>C (p.His736Pro) n.2768A>C n.358A>C | dbSNP |
| 1 | g.156881566A>G | CA1169631 | NTRK1 | c.2135A>G (p.His712Arg) c.*907A>G (n.*907A>G) c.2315A>G (p.His772Arg) c.374A>G c.2306A>G (p.His769Arg) c.2297A>G (p.His766Arg) c.2207A>G (p.His736Arg) n.2768A>G n.358A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881566A>T | CA342941673 | NTRK1 | c.2135A>T (p.His712Leu) c.*907A>T (n.*907A>T) c.2315A>T (p.His772Leu) c.374A>T c.2306A>T (p.His769Leu) c.2297A>T (p.His766Leu) c.2207A>T (p.His736Leu) n.2768A>T n.358A>T | dbSNP |
| 1 | g.156881567C>A | CA342941675 | NTRK1 | c.2136C>A (p.His712Gln) c.*908C>A (n.*908C>A) c.2316C>A (p.His772Gln) c.375C>A c.2307C>A (p.His769Gln) c.2298C>A (p.His766Gln) c.2208C>A (p.His736Gln) n.2769C>A n.359C>A | dbSNP |
| 1 | g.156881567C= | CA1200788870 | NTRK1 | c.2136C= (p.His712=) c.*908C= (n.*908C=) c.2316C= (p.His772=) c.375C= c.2307C= (p.His769=) c.2298C= (p.His766=) c.2208C= (p.His736=) n.2769C= n.359C= | |
| 1 | g.156881567C>G | CA342941676 | NTRK1 | c.2136C>G (p.His712Gln) c.*908C>G (n.*908C>G) c.2316C>G (p.His772Gln) c.375C>G c.2307C>G (p.His769Gln) c.2298C>G (p.His766Gln) c.2208C>G (p.His736Gln) n.2769C>G n.359C>G | dbSNP |
| 1 | g.156881567C>T | CA31126188 | NTRK1 | c.2136C>T (p.His712=) c.*908C>T (n.*908C>T) c.2316C>T (p.His772=) c.375C>T c.2307C>T (p.His769=) c.2298C>T (p.His766=) c.2208C>T (p.His736=) n.2769C>T n.359C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881568A>C | CA342941678 | NTRK1 | c.2137A>C (p.Ser713Arg) c.*909A>C (n.*909A>C) c.2317A>C (p.Ser773Arg) c.376A>C c.2308A>C (p.Ser770Arg) c.2299A>C (p.Ser767Arg) c.2209A>C (p.Ser737Arg) n.2770A>C n.360A>C | |
| 1 | g.156881568A>G | CA342941679 | NTRK1 | c.2137A>G (p.Ser713Gly) c.*909A>G (n.*909A>G) c.2317A>G (p.Ser773Gly) c.376A>G c.2308A>G (p.Ser770Gly) c.2299A>G (p.Ser767Gly) c.2209A>G (p.Ser737Gly) n.2770A>G n.360A>G | dbSNP gnomAD v4 |
| 1 | g.156881568A>T | CA342941680 | NTRK1 | c.2137A>T (p.Ser713Cys) c.*909A>T (n.*909A>T) c.2317A>T (p.Ser773Cys) c.376A>T c.2308A>T (p.Ser770Cys) c.2299A>T (p.Ser767Cys) c.2209A>T (p.Ser737Cys) n.2770A>T n.360A>T | dbSNP |
| 1 | g.156881569G>A | CA342941682 | NTRK1 | c.2138G>A (p.Ser713Asn) c.*910G>A (n.*910G>A) c.2318G>A (p.Ser773Asn) c.377G>A c.2309G>A (p.Ser770Asn) c.2300G>A (p.Ser767Asn) c.2210G>A (p.Ser737Asn) n.2771G>A n.361G>A | dbSNP gnomAD v4 COSMIC COSMIC |
| 1 | g.156881569G>C | CA342941683 | NTRK1 | c.2138G>C (p.Ser713Thr) c.*910G>C (n.*910G>C) c.2318G>C (p.Ser773Thr) c.377G>C c.2309G>C (p.Ser770Thr) c.2300G>C (p.Ser767Thr) c.2210G>C (p.Ser737Thr) n.2771G>C n.361G>C | dbSNP gnomAD v4 |
| 1 | g.156881569G>T | CA342941684 | NTRK1 | c.2138G>T (p.Ser713Ile) c.*910G>T (n.*910G>T) c.2318G>T (p.Ser773Ile) c.377G>T c.2309G>T (p.Ser770Ile) c.2300G>T (p.Ser767Ile) c.2210G>T (p.Ser737Ile) n.2771G>T n.361G>T | gnomAD v4 |
| 1 | g.156881570C>A | CA342941685 | NTRK1 | c.2139C>A (p.Ser713Arg) c.*911C>A (n.*911C>A) c.2319C>A (p.Ser773Arg) c.378C>A c.2310C>A (p.Ser770Arg) c.2301C>A (p.Ser767Arg) c.2211C>A (p.Ser737Arg) n.2772C>A n.362C>A | dbSNP gnomAD v4 |
| 1 | g.156881570C>G | CA342941686 | NTRK1 | c.2139C>G (p.Ser713Arg) c.*911C>G (n.*911C>G) c.2319C>G (p.Ser773Arg) c.378C>G c.2310C>G (p.Ser770Arg) c.2301C>G (p.Ser767Arg) c.2211C>G (p.Ser737Arg) n.2772C>G n.362C>G | dbSNP |
| 1 | g.156881570C>T | CA421140661 | NTRK1 | c.2139C>T (p.Ser713=) c.*911C>T (n.*911C>T) c.2319C>T (p.Ser773=) c.378C>T c.2310C>T (p.Ser770=) c.2301C>T (p.Ser767=) c.2211C>T (p.Ser737=) n.2772C>T n.362C>T | ClinVar dbSNP |
| 1 | g.156881571A>C | CA342941688 | NTRK1 | c.2140A>C (p.Ile714Leu) c.*912A>C (n.*912A>C) c.2320A>C (p.Ile774Leu) c.379A>C c.2311A>C (p.Ile771Leu) c.2302A>C (p.Ile768Leu) c.2212A>C (p.Ile738Leu) n.2773A>C n.363A>C | dbSNP |
| 1 | g.156881571A>G | CA342941690 | NTRK1 | c.2140A>G (p.Ile714Val) c.*912A>G (n.*912A>G) c.2320A>G (p.Ile774Val) c.379A>G c.2311A>G (p.Ile771Val) c.2302A>G (p.Ile768Val) c.2212A>G (p.Ile738Val) n.2773A>G n.363A>G | |
| 1 | g.156881571A>T | CA342941689 | NTRK1 | c.2140A>T (p.Ile714Phe) c.*912A>T (n.*912A>T) c.2320A>T (p.Ile774Phe) c.379A>T c.2311A>T (p.Ile771Phe) c.2302A>T (p.Ile768Phe) c.2212A>T (p.Ile738Phe) n.2773A>T n.363A>T | |
| 1 | g.156881572T>A | CA342941692 | NTRK1 | c.2141T>A (p.Ile714Asn) c.*913T>A (n.*913T>A) c.2321T>A (p.Ile774Asn) c.380T>A c.2312T>A (p.Ile771Asn) c.2303T>A (p.Ile768Asn) c.2213T>A (p.Ile738Asn) n.2774T>A n.364T>A | dbSNP |
| 1 | g.156881572T>C | CA342941693 | NTRK1 | c.2141T>C (p.Ile714Thr) c.*913T>C (n.*913T>C) c.2321T>C (p.Ile774Thr) c.380T>C c.2312T>C (p.Ile771Thr) c.2303T>C (p.Ile768Thr) c.2213T>C (p.Ile738Thr) n.2774T>C n.364T>C | gnomAD v4 |
| 1 | g.156881572T>G | CA342941694 | NTRK1 | c.2141T>G (p.Ile714Ser) c.*913T>G (n.*913T>G) c.2321T>G (p.Ile774Ser) c.380T>G c.2312T>G (p.Ile771Ser) c.2303T>G (p.Ile768Ser) c.2213T>G (p.Ile738Ser) n.2774T>G n.364T>G | dbSNP |
| 1 | g.156881573C>A | CA421140662 | NTRK1 | c.2142C>A (p.Ile714=) c.*914C>A (n.*914C>A) c.2322C>A (p.Ile774=) c.381C>A c.2313C>A (p.Ile771=) c.2304C>A (p.Ile768=) c.2214C>A (p.Ile738=) n.2775C>A n.365C>A | dbSNP |
| 1 | g.156881573C>G | CA342941695 | NTRK1 | c.2142C>G (p.Ile714Met) c.*914C>G (n.*914C>G) c.2322C>G (p.Ile774Met) c.381C>G c.2313C>G (p.Ile771Met) c.2304C>G (p.Ile768Met) c.2214C>G (p.Ile738Met) n.2775C>G n.365C>G | dbSNP |
| 1 | g.156881573C>T | CA421140663 | NTRK1 | c.2142C>T (p.Ile714=) c.*914C>T (n.*914C>T) c.2322C>T (p.Ile774=) c.381C>T c.2313C>T (p.Ile771=) c.2304C>T (p.Ile768=) c.2214C>T (p.Ile738=) n.2775C>T n.365C>T | dbSNP |
| 1 | g.156881574A= | CA1200788874 | NTRK1 | c.2143A= (p.Lys715=) c.*915A= (n.*915A=) c.2323A= (p.Lys775=) c.382A= c.2314A= (p.Lys772=) c.2305A= (p.Lys769=) c.2215A= (p.Lys739=) n.2776A= n.366A= | |
| 1 | g.156881574A>C | CA342941696 | NTRK1 | c.2143A>C (p.Lys715Gln) c.*915A>C (n.*915A>C) c.2323A>C (p.Lys775Gln) c.382A>C c.2314A>C (p.Lys772Gln) c.2305A>C (p.Lys769Gln) c.2215A>C (p.Lys739Gln) n.2776A>C n.366A>C | |
| 1 | g.156881574A>G | CA342941697 | NTRK1 | c.2143A>G (p.Lys715Glu) c.*915A>G (n.*915A>G) c.2323A>G (p.Lys775Glu) c.382A>G c.2314A>G (p.Lys772Glu) c.2305A>G (p.Lys769Glu) c.2215A>G (p.Lys739Glu) n.2776A>G n.366A>G | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156881574A>T | CA342941698 | NTRK1 | c.2143A>T (p.Lys715Ter) c.*915A>T (n.*915A>T) c.2323A>T (p.Lys775Ter) c.382A>T c.2314A>T (p.Lys772Ter) c.2305A>T (p.Lys769Ter) c.2215A>T (p.Lys739Ter) n.2776A>T n.366A>T | dbSNP |
| 1 | g.156881575A= | CA1200788883 | NTRK1 | c.2144A= (p.Lys715=) c.*916A= (n.*916A=) c.2324A= (p.Lys775=) c.383A= c.2315A= (p.Lys772=) c.2306A= (p.Lys769=) c.2216A= (p.Lys739=) n.2777A= n.367A= | |
| 1 | g.156881575A>C | CA342941699 | NTRK1 | c.2144A>C (p.Lys715Thr) c.*916A>C (n.*916A>C) c.2324A>C (p.Lys775Thr) c.383A>C c.2315A>C (p.Lys772Thr) c.2306A>C (p.Lys769Thr) c.2216A>C (p.Lys739Thr) n.2777A>C n.367A>C | |
| 1 | g.156881575A>G | CA342941700 | NTRK1 | c.2144A>G (p.Lys715Arg) c.*916A>G (n.*916A>G) c.2324A>G (p.Lys775Arg) c.383A>G c.2315A>G (p.Lys772Arg) c.2306A>G (p.Lys769Arg) c.2216A>G (p.Lys739Arg) n.2777A>G n.367A>G | ClinVar dbSNP |
| 1 | g.156881575A>T | CA342941701 | NTRK1 | c.2144A>T (p.Lys715Met) c.*916A>T (n.*916A>T) c.2324A>T (p.Lys775Met) c.383A>T c.2315A>T (p.Lys772Met) c.2306A>T (p.Lys769Met) c.2216A>T (p.Lys739Met) n.2777A>T n.367A>T | dbSNP |
| 1 | g.156881576G>A | CA1169632 | NTRK1 | c.2145G>A (p.Lys715=) c.*917G>A (n.*917G>A) c.2325G>A (p.Lys775=) c.384G>A c.2316G>A (p.Lys772=) c.2307G>A (p.Lys769=) c.2217G>A (p.Lys739=) n.2778G>A n.368G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881576G>C | CA342941703 | NTRK1 | c.2145G>C (p.Lys715Asn) c.*917G>C (n.*917G>C) c.2325G>C (p.Lys775Asn) c.384G>C c.2316G>C (p.Lys772Asn) c.2307G>C (p.Lys769Asn) c.2217G>C (p.Lys739Asn) n.2778G>C n.368G>C | |
| 1 | g.156881576G= | CA1147565605 | NTRK1 | c.2145G= (p.Lys715=) c.*917G= (n.*917G=) c.2325G= (p.Lys775=) c.384G= c.2316G= (p.Lys772=) c.2307G= (p.Lys769=) c.2217G= (p.Lys739=) n.2778G= n.368G= | |
| 1 | g.156881576G>T | CA342941702 | NTRK1 | c.2145G>T (p.Lys715Asn) c.*917G>T (n.*917G>T) c.2325G>T (p.Lys775Asn) c.384G>T c.2316G>T (p.Lys772Asn) c.2307G>T (p.Lys769Asn) c.2217G>T (p.Lys739Asn) n.2778G>T n.368G>T | dbSNP |
| 1 | g.156881577G>A | CA342941705 | NTRK1 | c.2146G>A (p.Asp716Asn) c.*918G>A (n.*918G>A) c.2326G>A (p.Asp776Asn) c.385G>A c.2317G>A (p.Asp773Asn) c.2308G>A (p.Asp770Asn) c.2218G>A (p.Asp740Asn) n.2779G>A n.369G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881577G>C | CA342941708 | NTRK1 | c.2146G>C (p.Asp716His) c.*918G>C (n.*918G>C) c.2326G>C (p.Asp776His) c.385G>C c.2317G>C (p.Asp773His) c.2308G>C (p.Asp770His) c.2218G>C (p.Asp740His) n.2779G>C n.369G>C | dbSNP gnomAD v4 |
| 1 | g.156881577G= | CA1200788890 | NTRK1 | c.2146G= (p.Asp716=) c.*918G= (n.*918G=) c.2326G= (p.Asp776=) c.385G= c.2317G= (p.Asp773=) c.2308G= (p.Asp770=) c.2218G= (p.Asp740=) n.2779G= n.369G= | |
| 1 | g.156881577G>T | CA342941706 | NTRK1 | c.2146G>T (p.Asp716Tyr) c.*918G>T (n.*918G>T) c.2326G>T (p.Asp776Tyr) c.385G>T c.2317G>T (p.Asp773Tyr) c.2308G>T (p.Asp770Tyr) c.2218G>T (p.Asp740Tyr) n.2779G>T n.369G>T | dbSNP gnomAD v4 |
| 1 | g.156881578A= | CA1148429413 | NTRK1 | c.2147A= (p.Asp716=) c.*919A= (n.*919A=) c.2327A= (p.Asp776=) c.386A= c.2318A= (p.Asp773=) c.2309A= (p.Asp770=) c.2219A= (p.Asp740=) n.2780A= n.370A= | |
| 1 | g.156881578A>C | CA342941709 | NTRK1 | c.2147A>C (p.Asp716Ala) c.*919A>C (n.*919A>C) c.2327A>C (p.Asp776Ala) c.386A>C c.2318A>C (p.Asp773Ala) c.2309A>C (p.Asp770Ala) c.2219A>C (p.Asp740Ala) n.2780A>C n.370A>C | |
| 1 | g.156881578A>G | CA342941710 | NTRK1 | c.2147A>G (p.Asp716Gly) c.*919A>G (n.*919A>G) c.2327A>G (p.Asp776Gly) c.386A>G c.2318A>G (p.Asp773Gly) c.2309A>G (p.Asp770Gly) c.2219A>G (p.Asp740Gly) n.2780A>G n.370A>G | |
| 1 | g.156881578A>T | CA1169633 | NTRK1 | c.2147A>T (p.Asp716Val) c.*919A>T (n.*919A>T) c.2327A>T (p.Asp776Val) c.386A>T c.2318A>T (p.Asp773Val) c.2309A>T (p.Asp770Val) c.2219A>T (p.Asp740Val) n.2780A>T n.370A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881579T>A | CA342941711 | NTRK1 | c.2148T>A (p.Asp716Glu) c.*920T>A (n.*920T>A) c.2328T>A (p.Asp776Glu) c.387T>A c.2319T>A (p.Asp773Glu) c.2310T>A (p.Asp770Glu) c.2220T>A (p.Asp740Glu) n.2781T>A n.371T>A | |
| 1 | g.156881579T>C | CA421140664 | NTRK1 | c.2148T>C (p.Asp716=) c.*920T>C (n.*920T>C) c.2328T>C (p.Asp776=) c.387T>C c.2319T>C (p.Asp773=) c.2310T>C (p.Asp770=) c.2220T>C (p.Asp740=) n.2781T>C n.371T>C | ClinVar dbSNP |
| 1 | g.156881579T>G | CA342941712 | NTRK1 | c.2148T>G (p.Asp716Glu) c.*920T>G (n.*920T>G) c.2328T>G (p.Asp776Glu) c.387T>G c.2319T>G (p.Asp773Glu) c.2310T>G (p.Asp770Glu) c.2220T>G (p.Asp740Glu) n.2781T>G n.371T>G | dbSNP COSMIC |
| 1 | g.156881579dup | CA915941479 | NTRK1 | c.2148dup (p.Val717CysfsTer?) c.*920dup (n.*920dup) c.2328dup (p.Val777CysfsTer?) c.387dup c.2319dup (p.Val774CysfsTer?) c.2310dup (p.Val771CysfsTer?) c.2220dup (p.Val741CysfsTer?) n.2781dup n.371dup | ClinVar dbSNP |
| 1 | g.156881580G>A | CA342941715 | NTRK1 | c.2149G>A (p.Val717Met) c.*921G>A (n.*921G>A) c.2329G>A (p.Val777Met) c.388G>A c.2320G>A (p.Val774Met) c.2311G>A (p.Val771Met) c.2221G>A (p.Val741Met) n.2782G>A n.372G>A | |
| 1 | g.156881580G>C | CA342941714 | NTRK1 | c.2149G>C (p.Val717Leu) c.*921G>C (n.*921G>C) c.2329G>C (p.Val777Leu) c.388G>C c.2320G>C (p.Val774Leu) c.2311G>C (p.Val771Leu) c.2221G>C (p.Val741Leu) n.2782G>C n.372G>C | |
| 1 | g.156881580G>T | CA342941713 | NTRK1 | c.2149G>T (p.Val717Leu) c.*921G>T (n.*921G>T) c.2329G>T (p.Val777Leu) c.388G>T c.2320G>T (p.Val774Leu) c.2311G>T (p.Val771Leu) c.2221G>T (p.Val741Leu) n.2782G>T n.372G>T | |
| 1 | g.156881581T>A | CA342941716 | NTRK1 | c.2150T>A (p.Val717Glu) c.*922T>A (n.*922T>A) c.2330T>A (p.Val777Glu) c.389T>A c.2321T>A (p.Val774Glu) c.2312T>A (p.Val771Glu) c.2222T>A (p.Val741Glu) n.2783T>A n.373T>A | dbSNP |
| 1 | g.156881581T>C | CA342941717 | NTRK1 | c.2150T>C (p.Val717Ala) c.*922T>C (n.*922T>C) c.2330T>C (p.Val777Ala) c.389T>C c.2321T>C (p.Val774Ala) c.2312T>C (p.Val771Ala) c.2222T>C (p.Val741Ala) n.2783T>C n.373T>C | |
| 1 | g.156881581T>G | CA342941718 | NTRK1 | c.2150T>G (p.Val717Gly) c.*922T>G (n.*922T>G) c.2330T>G (p.Val777Gly) c.389T>G c.2321T>G (p.Val774Gly) c.2312T>G (p.Val771Gly) c.2222T>G (p.Val741Gly) n.2783T>G n.373T>G | dbSNP |
| 1 | g.156881581_156881609delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG | CA1200788906 | NTRK1 | c.2150_2178delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val717=) c.*922_*950delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (n.*922_*950delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG) c.2330_2358delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val777=) c.389_417delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG c.2321_2349delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val774=) c.2312_2340delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val771=) c.2222_2250delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val741=) n.2783_2811delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG n.373_401delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG | |
| 1 | g.156881582G>A | CA421140665 | NTRK1 | c.2151G>A (p.Val717=) c.*923G>A (n.*923G>A) c.2331G>A (p.Val777=) c.390G>A c.2322G>A (p.Val774=) c.2313G>A (p.Val771=) c.2223G>A (p.Val741=) n.2784G>A n.374G>A | dbSNP |
| 1 | g.156881582G>C | CA421140666 | NTRK1 | c.2151G>C (p.Val717=) c.*923G>C (n.*923G>C) c.2331G>C (p.Val777=) c.390G>C c.2322G>C (p.Val774=) c.2313G>C (p.Val771=) c.2223G>C (p.Val741=) n.2784G>C n.374G>C | dbSNP |
| 1 | g.156881582G>T | CA421140667 | NTRK1 | c.2151G>T (p.Val717=) c.*923G>T (n.*923G>T) c.2331G>T (p.Val777=) c.390G>T c.2322G>T (p.Val774=) c.2313G>T (p.Val771=) c.2223G>T (p.Val741=) n.2784G>T n.374G>T | gnomAD v4 |
| 1 | g.156881586_156881613del | CA891843047 | NTRK1 | c.2155_2182del (p.Ala719LeufsTer?) c.*927_*954del (n.*927_*954del) c.2335_2362del (p.Ala779LeufsTer?) c.394_421del c.2326_2353del (p.Ala776LeufsTer?) c.2317_2344del (p.Ala773LeufsTer?) c.2227_2254del (p.Ala743LeufsTer?) n.2788_2815del n.378_405del | ClinVar dbSNP |
| 1 | g.156881583C>A | CA342941719 | NTRK1 | c.2152C>A (p.His718Asn) c.*924C>A (n.*924C>A) c.2332C>A (p.His778Asn) c.391C>A c.2323C>A (p.His775Asn) c.2314C>A (p.His772Asn) c.2224C>A (p.His742Asn) n.2785C>A n.375C>A | |
| 1 | g.156881583C>G | CA342941720 | NTRK1 | c.2152C>G (p.His718Asp) c.*924C>G (n.*924C>G) c.2332C>G (p.His778Asp) c.391C>G c.2323C>G (p.His775Asp) c.2314C>G (p.His772Asp) c.2224C>G (p.His742Asp) n.2785C>G n.375C>G | dbSNP |
| 1 | g.156881583C>T | CA342941721 | NTRK1 | c.2152C>T (p.His718Tyr) c.*924C>T (n.*924C>T) c.2332C>T (p.His778Tyr) c.391C>T c.2323C>T (p.His775Tyr) c.2314C>T (p.His772Tyr) c.2224C>T (p.His742Tyr) n.2785C>T n.375C>T | dbSNP gnomAD v4 |
| 1 | g.156881584A>C | CA342941722 | NTRK1 | c.2153A>C (p.His718Pro) c.*925A>C (n.*925A>C) c.2333A>C (p.His778Pro) c.392A>C c.2324A>C (p.His775Pro) c.2315A>C (p.His772Pro) c.2225A>C (p.His742Pro) n.2786A>C n.376A>C | dbSNP |
| 1 | g.156881584A>G | CA342941724 | NTRK1 | c.2153A>G (p.His718Arg) c.*925A>G (n.*925A>G) c.2333A>G (p.His778Arg) c.392A>G c.2324A>G (p.His775Arg) c.2315A>G (p.His772Arg) c.2225A>G (p.His742Arg) n.2786A>G n.376A>G | dbSNP gnomAD v4 |
| 1 | g.156881584A>T | CA342941723 | NTRK1 | c.2153A>T (p.His718Leu) c.*925A>T (n.*925A>T) c.2333A>T (p.His778Leu) c.392A>T c.2324A>T (p.His775Leu) c.2315A>T (p.His772Leu) c.2225A>T (p.His742Leu) n.2786A>T n.376A>T | dbSNP |
| 1 | g.156881585C>A | CA342941725 | NTRK1 | c.2154C>A (p.His718Gln) c.*926C>A (n.*926C>A) c.2334C>A (p.His778Gln) c.393C>A c.2325C>A (p.His775Gln) c.2316C>A (p.His772Gln) c.2226C>A (p.His742Gln) n.2787C>A n.377C>A | dbSNP gnomAD v2 |
| 1 | g.156881585C= | CA1143734134 | NTRK1 | c.2154C= (p.His718=) c.*926C= (n.*926C=) c.2334C= (p.His778=) c.393C= c.2325C= (p.His775=) c.2316C= (p.His772=) c.2226C= (p.His742=) n.2787C= n.377C= | |
| 1 | g.156881585C>G | CA342941726 | NTRK1 | c.2154C>G (p.His718Gln) c.*926C>G (n.*926C>G) c.2334C>G (p.His778Gln) c.393C>G c.2325C>G (p.His775Gln) c.2316C>G (p.His772Gln) c.2226C>G (p.His742Gln) n.2787C>G n.377C>G | dbSNP |
| 1 | g.156881585C>T | CA1169634 | NTRK1 | c.2154C>T (p.His718=) c.*926C>T (n.*926C>T) c.2334C>T (p.His778=) c.393C>T c.2325C>T (p.His775=) c.2316C>T (p.His772=) c.2226C>T (p.His742=) n.2787C>T n.377C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.156881586G>A | CA1169635 | NTRK1 | c.2155G>A (p.Ala719Thr) c.*927G>A (n.*927G>A) c.2335G>A (p.Ala779Thr) c.394G>A c.2326G>A (p.Ala776Thr) c.2317G>A (p.Ala773Thr) c.2227G>A (p.Ala743Thr) n.2788G>A n.378G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881586G>C | CA342941727 | NTRK1 | c.2155G>C (p.Ala719Pro) c.*927G>C (n.*927G>C) c.2335G>C (p.Ala779Pro) c.394G>C c.2326G>C (p.Ala776Pro) c.2317G>C (p.Ala773Pro) c.2227G>C (p.Ala743Pro) n.2788G>C n.378G>C | dbSNP |
| 1 | g.156881586G= | CA1144028342 | NTRK1 | c.2155G= (p.Ala719=) c.*927G= (n.*927G=) c.2335G= (p.Ala779=) c.394G= c.2326G= (p.Ala776=) c.2317G= (p.Ala773=) c.2227G= (p.Ala743=) n.2788G= n.378G= | |
| 1 | g.156881586G>T | CA342941729 | NTRK1 | c.2155G>T (p.Ala719Ser) c.*927G>T (n.*927G>T) c.2335G>T (p.Ala779Ser) c.394G>T c.2326G>T (p.Ala776Ser) c.2317G>T (p.Ala773Ser) c.2227G>T (p.Ala743Ser) n.2788G>T n.378G>T | dbSNP gnomAD v4 |
| 1 | g.156881590_156881601del | CA2648467752 | NTRK1 | c.2159_2170del (p.Arg720_Ala723del) c.*931_*942del (n.*931_*942del) c.2339_2350del (p.Arg780_Ala783del) c.398_409del c.2330_2341del (p.Arg777_Ala780del) c.2321_2332del (p.Arg774_Ala777del) c.2231_2242del (p.Arg744_Ala747del) n.2792_2803del n.382_393del | gnomAD v4 |
| 1 | g.156881587C>A | CA342941730 | NTRK1 | c.2156C>A (p.Ala719Asp) c.*928C>A (n.*928C>A) c.2336C>A (p.Ala779Asp) c.395C>A c.2327C>A (p.Ala776Asp) c.2318C>A (p.Ala773Asp) c.2228C>A (p.Ala743Asp) n.2789C>A n.379C>A | |
| 1 | g.156881587C= | CA1200788924 | NTRK1 | c.2156C= (p.Ala719=) c.*928C= (n.*928C=) c.2336C= (p.Ala779=) c.395C= c.2327C= (p.Ala776=) c.2318C= (p.Ala773=) c.2228C= (p.Ala743=) n.2789C= n.379C= | |
| 1 | g.156881587C>G | CA342941731 | NTRK1 | c.2156C>G (p.Ala719Gly) c.*928C>G (n.*928C>G) c.2336C>G (p.Ala779Gly) c.395C>G c.2327C>G (p.Ala776Gly) c.2318C>G (p.Ala773Gly) c.2228C>G (p.Ala743Gly) n.2789C>G n.379C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881587C>T | CA342941732 | NTRK1 | c.2156C>T (p.Ala719Val) c.*928C>T (n.*928C>T) c.2336C>T (p.Ala779Val) c.395C>T c.2327C>T (p.Ala776Val) c.2318C>T (p.Ala773Val) c.2228C>T (p.Ala743Val) n.2789C>T n.379C>T | dbSNP |
| 1 | g.156881588C>A | CA421140670 | NTRK1 | c.2157C>A (p.Ala719=) c.*929C>A (n.*929C>A) c.2337C>A (p.Ala779=) c.396C>A c.2328C>A (p.Ala776=) c.2319C>A (p.Ala773=) c.2229C>A (p.Ala743=) n.2790C>A n.380C>A | gnomAD v4 |
| 1 | g.156881588C>G | CA421140669 | NTRK1 | c.2157C>G (p.Ala719=) c.*929C>G (n.*929C>G) c.2337C>G (p.Ala779=) c.396C>G c.2328C>G (p.Ala776=) c.2319C>G (p.Ala773=) c.2229C>G (p.Ala743=) n.2790C>G n.380C>G | |
| 1 | g.156881588C>T | CA421140668 | NTRK1 | c.2157C>T (p.Ala719=) c.*929C>T (n.*929C>T) c.2337C>T (p.Ala779=) c.396C>T c.2328C>T (p.Ala776=) c.2319C>T (p.Ala773=) c.2229C>T (p.Ala743=) n.2790C>T n.380C>T | |
| 1 | g.156881589C>A | CA421140671 | NTRK1 | c.2158C>A (p.Arg720=) c.*930C>A (n.*930C>A) c.2338C>A (p.Arg780=) c.397C>A c.2329C>A (p.Arg777=) c.2320C>A (p.Arg774=) c.2230C>A (p.Arg744=) n.2791C>A n.381C>A | dbSNP gnomAD v4 |
| 1 | g.156881589C= | CA1145049910 | NTRK1 | c.2158C= (p.Arg720=) c.*930C= (n.*930C=) c.2338C= (p.Arg780=) c.397C= c.2329C= (p.Arg777=) c.2320C= (p.Arg774=) c.2230C= (p.Arg744=) n.2791C= n.381C= | |
| 1 | g.156881589C>G | CA342941733 | NTRK1 | c.2158C>G (p.Arg720Gly) c.*930C>G (n.*930C>G) c.2338C>G (p.Arg780Gly) c.397C>G c.2329C>G (p.Arg777Gly) c.2320C>G (p.Arg774Gly) c.2230C>G (p.Arg744Gly) n.2791C>G n.381C>G | dbSNP gnomAD v4 COSMIC |
| 1 | g.156881589C>T | CA1169636 | NTRK1 | c.2158C>T (p.Arg720Trp) c.*930C>T (n.*930C>T) c.2338C>T (p.Arg780Trp) c.397C>T c.2329C>T (p.Arg777Trp) c.2320C>T (p.Arg774Trp) c.2230C>T (p.Arg744Trp) n.2791C>T n.381C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881590G>A | CA1169637 | NTRK1 | c.2159G>A (p.Arg720Gln) c.*931G>A (n.*931G>A) c.2339G>A (p.Arg780Gln) c.398G>A c.2330G>A (p.Arg777Gln) c.2321G>A (p.Arg774Gln) c.2231G>A (p.Arg744Gln) n.2792G>A n.382G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156881590G>C | CA256268 | NTRK1 | c.2159G>C (p.Arg720Pro) c.*931G>C (n.*931G>C) c.2339G>C (p.Arg780Pro) c.398G>C c.2330G>C (p.Arg777Pro) c.2321G>C (p.Arg774Pro) c.2231G>C (p.Arg744Pro) n.2792G>C n.382G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156881590G= | CA1140584233 | NTRK1 | c.2159G= (p.Arg720=) c.*931G= (n.*931G=) c.2339G= (p.Arg780=) c.398G= c.2330G= (p.Arg777=) c.2321G= (p.Arg774=) c.2231G= (p.Arg744=) n.2792G= n.382G= | |
| 1 | g.156881590G>T | CA342941734 | NTRK1 | c.2159G>T (p.Arg720Leu) c.*931G>T (n.*931G>T) c.2339G>T (p.Arg780Leu) c.398G>T c.2330G>T (p.Arg777Leu) c.2321G>T (p.Arg774Leu) c.2231G>T (p.Arg744Leu) n.2792G>T n.382G>T | gnomAD v4 |
| 1 | g.156881591G>A | CA1169638 | NTRK1 | c.2160G>A (p.Arg720=) c.*932G>A (n.*932G>A) c.2340G>A (p.Arg780=) c.399G>A c.2331G>A (p.Arg777=) c.2322G>A (p.Arg774=) c.2232G>A (p.Arg744=) n.2793G>A n.383G>A | ClinVar dbSNP ExAC gnomAD v2 |
| 1 | g.156881591G>C | CA421140673 | NTRK1 | c.2160G>C (p.Arg720=) c.*932G>C (n.*932G>C) c.2340G>C (p.Arg780=) c.399G>C c.2331G>C (p.Arg777=) c.2322G>C (p.Arg774=) c.2232G>C (p.Arg744=) n.2793G>C n.383G>C | dbSNP |
| 1 | g.156881591G= | CA1148269761 | NTRK1 | c.2160G= (p.Arg720=) c.*932G= (n.*932G=) c.2340G= (p.Arg780=) c.399G= c.2331G= (p.Arg777=) c.2322G= (p.Arg774=) c.2232G= (p.Arg744=) n.2793G= n.383G= | |
| 1 | g.156881591G>T | CA421140672 | NTRK1 | c.2160G>T (p.Arg720=) c.*932G>T (n.*932G>T) c.2340G>T (p.Arg780=) c.399G>T c.2331G>T (p.Arg777=) c.2322G>T (p.Arg774=) c.2232G>T (p.Arg744=) n.2793G>T n.383G>T |