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.156876412_156876422del | CA526673649 | NTRK1 | c.1465_1475del (p.Ala489CysfsTer8) c.*237_*247del (n.*237_*247del) c.1645_1655del (p.Ala549CysfsTer8) c.1636_1646del (p.Ala546CysfsTer8) c.1627_1637del (p.Ala543CysfsTer8) c.1537_1547del (p.Ala513CysfsTer8) n.2098_2108del | gnomAD v2 gnomAD v4 |
| 1 | g.156876419del | CA2586964226 | NTRK1 | c.1472del (p.Glu491GlyfsTer?) c.*244del (n.*244del) c.1652del (p.Glu551GlyfsTer?) c.1643del (p.Glu548GlyfsTer?) c.1634del (p.Glu545GlyfsTer?) c.1544del (p.Glu515GlyfsTer?) n.2105del | |
| 1 | g.156876419A= | CA1200786088 | NTRK1 | c.1472A= (p.Glu491=) c.*244A= (n.*244A=) c.1652A= (p.Glu551=) c.1643A= (p.Glu548=) c.1634A= (p.Glu545=) c.1544A= (p.Glu515=) n.2105A= | |
| 1 | g.156876419A>C | CA342938425 | NTRK1 | c.1472A>C (p.Glu491Ala) c.*244A>C (n.*244A>C) c.1652A>C (p.Glu551Ala) c.1643A>C (p.Glu548Ala) c.1634A>C (p.Glu545Ala) c.1544A>C (p.Glu515Ala) n.2105A>C | |
| 1 | g.156876419A>G | CA342938426 | NTRK1 | c.1472A>G (p.Glu491Gly) c.*244A>G (n.*244A>G) c.1652A>G (p.Glu551Gly) c.1643A>G (p.Glu548Gly) c.1634A>G (p.Glu545Gly) c.1544A>G (p.Glu515Gly) n.2105A>G | dbSNP |
| 1 | g.156876419A>T | CA342938427 | NTRK1 | c.1472A>T (p.Glu491Val) c.*244A>T (n.*244A>T) c.1652A>T (p.Glu551Val) c.1643A>T (p.Glu548Val) c.1634A>T (p.Glu545Val) c.1544A>T (p.Glu515Val) n.2105A>T | dbSNP |
| 1 | g.156876420G>A | CA421138522 | NTRK1 | c.1473G>A (p.Glu491=) c.*245G>A (n.*245G>A) c.1653G>A (p.Glu551=) c.1644G>A (p.Glu548=) c.1635G>A (p.Glu545=) c.1545G>A (p.Glu515=) n.2106G>A | dbSNP COSMIC |
| 1 | g.156876420G>C | CA342938428 | NTRK1 | c.1473G>C (p.Glu491Asp) c.*245G>C (n.*245G>C) c.1653G>C (p.Glu551Asp) c.1644G>C (p.Glu548Asp) c.1635G>C (p.Glu545Asp) c.1545G>C (p.Glu515Asp) n.2106G>C | dbSNP |
| 1 | g.156876420G>T | CA342938429 | NTRK1 | c.1473G>T (p.Glu491Asp) c.*245G>T (n.*245G>T) c.1653G>T (p.Glu551Asp) c.1644G>T (p.Glu548Asp) c.1635G>T (p.Glu545Asp) c.1545G>T (p.Glu515Asp) n.2106G>T | dbSNP |
| 1 | g.156876421A= | CA1200786089 | NTRK1 | c.1474A= (p.Ser492=) c.*246A= (n.*246A=) c.1654A= (p.Ser552=) c.1645A= (p.Ser549=) c.1636A= (p.Ser546=) c.1546A= (p.Ser516=) n.2107A= | |
| 1 | g.156876421A>C | CA342938430 | NTRK1 | c.1474A>C (p.Ser492Arg) c.*246A>C (n.*246A>C) c.1654A>C (p.Ser552Arg) c.1645A>C (p.Ser549Arg) c.1636A>C (p.Ser546Arg) c.1546A>C (p.Ser516Arg) n.2107A>C | |
| 1 | g.156876421A>G | CA1169432 | NTRK1 | c.1474A>G (p.Ser492Gly) c.*246A>G (n.*246A>G) c.1654A>G (p.Ser552Gly) c.1645A>G (p.Ser549Gly) c.1636A>G (p.Ser546Gly) c.1546A>G (p.Ser516Gly) n.2107A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876421A>T | CA342938431 | NTRK1 | c.1474A>T (p.Ser492Cys) c.*246A>T (n.*246A>T) c.1654A>T (p.Ser552Cys) c.1645A>T (p.Ser549Cys) c.1636A>T (p.Ser546Cys) c.1546A>T (p.Ser516Cys) n.2107A>T | dbSNP |
| 1 | g.156876422G>A | CA342938432 | NTRK1 | c.1475G>A (p.Ser492Asn) c.*247G>A (n.*247G>A) c.1655G>A (p.Ser552Asn) c.1646G>A (p.Ser549Asn) c.1637G>A (p.Ser546Asn) c.1547G>A (p.Ser516Asn) n.2108G>A | dbSNP |
| 1 | g.156876422G>C | CA342938433 | NTRK1 | c.1475G>C (p.Ser492Thr) c.*247G>C (n.*247G>C) c.1655G>C (p.Ser552Thr) c.1646G>C (p.Ser549Thr) c.1637G>C (p.Ser546Thr) c.1547G>C (p.Ser516Thr) n.2108G>C | dbSNP |
| 1 | g.156876422G>T | CA342938434 | NTRK1 | c.1475G>T (p.Ser492Ile) c.*247G>T (n.*247G>T) c.1655G>T (p.Ser552Ile) c.1646G>T (p.Ser549Ile) c.1637G>T (p.Ser546Ile) c.1547G>T (p.Ser516Ile) n.2108G>T | |
| 1 | g.156876423T>A | CA342938436 | NTRK1 | c.1476T>A (p.Ser492Arg) c.*248T>A (n.*248T>A) c.1656T>A (p.Ser552Arg) c.1647T>A (p.Ser549Arg) c.1638T>A (p.Ser546Arg) c.1548T>A (p.Ser516Arg) n.2109T>A | dbSNP |
| 1 | g.156876423T>C | CA421138537 | NTRK1 | c.1476T>C (p.Ser492=) c.*248T>C (n.*248T>C) c.1656T>C (p.Ser552=) c.1647T>C (p.Ser549=) c.1638T>C (p.Ser546=) c.1548T>C (p.Ser516=) n.2109T>C | gnomAD v4 |
| 1 | g.156876423T>G | CA342938435 | NTRK1 | c.1476T>G (p.Ser492Arg) c.*248T>G (n.*248T>G) c.1656T>G (p.Ser552Arg) c.1647T>G (p.Ser549Arg) c.1638T>G (p.Ser546Arg) c.1548T>G (p.Ser516Arg) n.2109T>G | dbSNP |
| 1 | g.156876423_156876424delinsTG | CA1200786090 | NTRK1 | c.1476_1477delinsTG (p.Ser492=) c.*248_*249delinsTG (n.*248_*249delinsTG) c.1656_1657delinsTG (p.Ser552=) c.1647_1648delinsTG (p.Ser549=) c.1638_1639delinsTG (p.Ser546=) c.1548_1549delinsTG (p.Ser516=) n.2109_2110delinsTG | |
| 1 | g.156876424del | CA1200786091 | NTRK1 | c.1477del (p.Ala493LeufsTer?) c.*249del (n.*249del) c.1657del (p.Ala553LeufsTer?) c.1648del (p.Ala550LeufsTer?) c.1639del (p.Ala547LeufsTer?) c.1549del (p.Ala517LeufsTer?) n.2110del | dbSNP |
| 1 | g.156876424G>A | CA342938437 | NTRK1 | c.1477G>A (p.Ala493Thr) c.*249G>A (n.*249G>A) c.1657G>A (p.Ala553Thr) c.1648G>A (p.Ala550Thr) c.1639G>A (p.Ala547Thr) c.1549G>A (p.Ala517Thr) n.2110G>A | dbSNP |
| 1 | g.156876424G>C | CA342938438 | NTRK1 | c.1477G>C (p.Ala493Pro) c.*249G>C (n.*249G>C) c.1657G>C (p.Ala553Pro) c.1648G>C (p.Ala550Pro) c.1639G>C (p.Ala547Pro) c.1549G>C (p.Ala517Pro) n.2110G>C | dbSNP |
| 1 | g.156876424G>T | CA342938439 | NTRK1 | c.1477G>T (p.Ala493Ser) c.*249G>T (n.*249G>T) c.1657G>T (p.Ala553Ser) c.1648G>T (p.Ala550Ser) c.1639G>T (p.Ala547Ser) c.1549G>T (p.Ala517Ser) n.2110G>T | |
| 1 | g.156876425C>A | CA342938440 | NTRK1 | c.1478C>A (p.Ala493Asp) c.*250C>A (n.*250C>A) c.1658C>A (p.Ala553Asp) c.1649C>A (p.Ala550Asp) c.1640C>A (p.Ala547Asp) c.1550C>A (p.Ala517Asp) n.2111C>A | |
| 1 | g.156876425C>G | CA342938441 | NTRK1 | c.1478C>G (p.Ala493Gly) c.*250C>G (n.*250C>G) c.1658C>G (p.Ala553Gly) c.1649C>G (p.Ala550Gly) c.1640C>G (p.Ala547Gly) c.1550C>G (p.Ala517Gly) n.2111C>G | dbSNP |
| 1 | g.156876425C>T | CA342938442 | NTRK1 | c.1478C>T (p.Ala493Val) c.*250C>T (n.*250C>T) c.1658C>T (p.Ala553Val) c.1649C>T (p.Ala550Val) c.1640C>T (p.Ala547Val) c.1550C>T (p.Ala517Val) n.2111C>T | dbSNP |
| 1 | g.156876425_156876426delinsCT | CA1200786092 | NTRK1 | c.1478_1479delinsCT (p.Ala493=) c.*250_*251delinsCT (n.*250_*251delinsCT) c.1658_1659delinsCT (p.Ala553=) c.1649_1650delinsCT (p.Ala550=) c.1640_1641delinsCT (p.Ala547=) c.1550_1551delinsCT (p.Ala517=) n.2111_2112delinsCT | |
| 1 | g.156876426del | CA889790049 | NTRK1 | c.1479del (p.Arg494GlyfsTer?) c.*251del (n.*251del) c.1659del (p.Arg554GlyfsTer?) c.1650del (p.Arg551GlyfsTer?) c.1641del (p.Arg548GlyfsTer?) c.1551del (p.Arg518GlyfsTer?) n.2112del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876426T>A | CA421138545 | NTRK1 | c.1479T>A (p.Ala493=) c.*251T>A (n.*251T>A) c.1659T>A (p.Ala553=) c.1650T>A (p.Ala550=) c.1641T>A (p.Ala547=) c.1551T>A (p.Ala517=) n.2112T>A | dbSNP |
| 1 | g.156876426T>C | CA421138547 | NTRK1 | c.1479T>C (p.Ala493=) c.*251T>C (n.*251T>C) c.1659T>C (p.Ala553=) c.1650T>C (p.Ala550=) c.1641T>C (p.Ala547=) c.1551T>C (p.Ala517=) n.2112T>C | ClinVar dbSNP |
| 1 | g.156876426T>G | CA421138549 | NTRK1 | c.1479T>G (p.Ala493=) c.*251T>G (n.*251T>G) c.1659T>G (p.Ala553=) c.1650T>G (p.Ala550=) c.1641T>G (p.Ala547=) c.1551T>G (p.Ala517=) n.2112T>G | |
| 1 | g.156876426_156876427delinsTC | CA1200786094 | NTRK1 | c.1479_1480delinsTC (p.Ala493=) c.*251_*252delinsTC (n.*251_*252delinsTC) c.1659_1660delinsTC (p.Ala553=) c.1650_1651delinsTC (p.Ala550=) c.1641_1642delinsTC (p.Ala547=) c.1551_1552delinsTC (p.Ala517=) n.2112_2113delinsTC | |
| 1 | g.156876426_156876438delinsTCGGCAGGACTTC | CA1200786093 | NTRK1 | c.1479_1491delinsTCGGCAGGACTTC (p.Ala493=) c.*251_*263delinsTCGGCAGGACTTC (n.*251_*263delinsTCGGCAGGACTTC) c.1659_1671delinsTCGGCAGGACTTC (p.Ala553=) c.1650_1662delinsTCGGCAGGACTTC (p.Ala550=) c.1641_1653delinsTCGGCAGGACTTC (p.Ala547=) c.1551_1563delinsTCGGCAGGACTTC (p.Ala517=) n.2112_2124delinsTCGGCAGGACTTC | |
| 1 | g.156876427del | CA341875 | NTRK1 | c.1480del (p.Arg494GlyfsTer?) c.*252del (n.*252del) c.1660del (p.Arg554GlyfsTer?) c.1651del (p.Arg551GlyfsTer?) c.1642del (p.Arg548GlyfsTer?) c.1552del (p.Arg518GlyfsTer?) n.2113del | ClinVar dbSNP gnomAD v4 |
| 1 | g.156876427C>A | CA421138552 | NTRK1 | c.1480C>A (p.Arg494=) c.*252C>A (n.*252C>A) c.1660C>A (p.Arg554=) c.1651C>A (p.Arg551=) c.1642C>A (p.Arg548=) c.1552C>A (p.Arg518=) n.2113C>A | dbSNP |
| 1 | g.156876427C= | CA1141188059 | NTRK1 | c.1480C= (p.Arg494=) c.*252C= (n.*252C=) c.1660C= (p.Arg554=) c.1651C= (p.Arg551=) c.1642C= (p.Arg548=) c.1552C= (p.Arg518=) n.2113C= | |
| 1 | g.156876427C>G | CA342938443 | NTRK1 | c.1480C>G (p.Arg494Gly) c.*252C>G (n.*252C>G) c.1660C>G (p.Arg554Gly) c.1651C>G (p.Arg551Gly) c.1642C>G (p.Arg548Gly) c.1552C>G (p.Arg518Gly) n.2113C>G | dbSNP gnomAD v4 |
| 1 | g.156876427C>T | CA1169433 | NTRK1 | c.1480C>T (p.Arg494Trp) c.*252C>T (n.*252C>T) c.1660C>T (p.Arg554Trp) c.1651C>T (p.Arg551Trp) c.1642C>T (p.Arg548Trp) c.1552C>T (p.Arg518Trp) n.2113C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876428_156876439del | CA889790057 | NTRK1 | c.1481_1492del (p.Arg494_Phe497del) c.*253_*264del (n.*253_*264del) c.1661_1672del (p.Arg554_Phe557del) c.1652_1663del (p.Arg551_Phe554del) c.1643_1654del (p.Arg548_Phe551del) c.1553_1564del (p.Arg518_Phe521del) n.2114_2125del | dbSNP |
| 1 | g.156876428G>A | CA1169434 | NTRK1 | c.1481G>A (p.Arg494Gln) c.*253G>A (n.*253G>A) c.1661G>A (p.Arg554Gln) c.1652G>A (p.Arg551Gln) c.1643G>A (p.Arg548Gln) c.1553G>A (p.Arg518Gln) n.2114G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876428G>C | CA31118730 | NTRK1 | c.1481G>C (p.Arg494Pro) c.*253G>C (n.*253G>C) c.1661G>C (p.Arg554Pro) c.1652G>C (p.Arg551Pro) c.1643G>C (p.Arg548Pro) c.1553G>C (p.Arg518Pro) n.2114G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876428G= | CA1200786095 | NTRK1 | c.1481G= (p.Arg494=) c.*253G= (n.*253G=) c.1661G= (p.Arg554=) c.1652G= (p.Arg551=) c.1643G= (p.Arg548=) c.1553G= (p.Arg518=) n.2114G= | |
| 1 | g.156876428G>T | CA342938444 | NTRK1 | c.1481G>T (p.Arg494Leu) c.*253G>T (n.*253G>T) c.1661G>T (p.Arg554Leu) c.1652G>T (p.Arg551Leu) c.1643G>T (p.Arg548Leu) c.1553G>T (p.Arg518Leu) n.2114G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876429G>A | CA421138564 | NTRK1 | c.1482G>A (p.Arg494=) c.*254G>A (n.*254G>A) c.1662G>A (p.Arg554=) c.1653G>A (p.Arg551=) c.1644G>A (p.Arg548=) c.1554G>A (p.Arg518=) n.2115G>A | dbSNP |
| 1 | g.156876429G>C | CA421138566 | NTRK1 | c.1482G>C (p.Arg494=) c.*254G>C (n.*254G>C) c.1662G>C (p.Arg554=) c.1653G>C (p.Arg551=) c.1644G>C (p.Arg548=) c.1554G>C (p.Arg518=) n.2115G>C | dbSNP |
| 1 | g.156876429G>T | CA421138567 | NTRK1 | c.1482G>T (p.Arg494=) c.*254G>T (n.*254G>T) c.1662G>T (p.Arg554=) c.1653G>T (p.Arg551=) c.1644G>T (p.Arg548=) c.1554G>T (p.Arg518=) n.2115G>T | ClinVar |
| 1 | g.156876430C>A | CA342938445 | NTRK1 | c.1483C>A (p.Gln495Lys) c.*255C>A (n.*255C>A) c.1663C>A (p.Gln555Lys) c.1654C>A (p.Gln552Lys) c.1645C>A (p.Gln549Lys) c.1555C>A (p.Gln519Lys) n.2116C>A | |
| 1 | g.156876430C= | CA1146945738 | NTRK1 | c.1483C= (p.Gln495=) c.*255C= (n.*255C=) c.1663C= (p.Gln555=) c.1654C= (p.Gln552=) c.1645C= (p.Gln549=) c.1555C= (p.Gln519=) n.2116C= | |
| 1 | g.156876430C>G | CA342938446 | NTRK1 | c.1483C>G (p.Gln495Glu) c.*255C>G (n.*255C>G) c.1663C>G (p.Gln555Glu) c.1654C>G (p.Gln552Glu) c.1645C>G (p.Gln549Glu) c.1555C>G (p.Gln519Glu) n.2116C>G | dbSNP |
| 1 | g.156876430C>T | CA31118740 | NTRK1 | c.1483C>T (p.Gln495Ter) c.*255C>T (n.*255C>T) c.1663C>T (p.Gln555Ter) c.1654C>T (p.Gln552Ter) c.1645C>T (p.Gln549Ter) c.1555C>T (p.Gln519Ter) n.2116C>T | dbSNP |
| 1 | g.156876433_156876441dup | CA2648464053 | NTRK1 | c.1486_1494dup (p.Gln498_Arg499insAspPheGln) c.*258_*266dup (n.*258_*266dup) c.1666_1674dup (p.Gln558_Arg559insAspPheGln) c.1657_1665dup (p.Gln555_Arg556insAspPheGln) c.1648_1656dup (p.Gln552_Arg553insAspPheGln) c.1558_1566dup (p.Gln522_Arg523insAspPheGln) n.2119_2127dup | gnomAD v4 |
| 1 | g.156876431A>C | CA342938447 | NTRK1 | c.1484A>C (p.Gln495Pro) c.*256A>C (n.*256A>C) c.1664A>C (p.Gln555Pro) c.1655A>C (p.Gln552Pro) c.1646A>C (p.Gln549Pro) c.1556A>C (p.Gln519Pro) n.2117A>C | |
| 1 | g.156876431A>G | CA342938448 | NTRK1 | c.1484A>G (p.Gln495Arg) c.*256A>G (n.*256A>G) c.1664A>G (p.Gln555Arg) c.1655A>G (p.Gln552Arg) c.1646A>G (p.Gln549Arg) c.1556A>G (p.Gln519Arg) n.2117A>G | dbSNP |
| 1 | g.156876431A>T | CA342938449 | NTRK1 | c.1484A>T (p.Gln495Leu) c.*256A>T (n.*256A>T) c.1664A>T (p.Gln555Leu) c.1655A>T (p.Gln552Leu) c.1646A>T (p.Gln549Leu) c.1556A>T (p.Gln519Leu) n.2117A>T | dbSNP |
| 1 | g.156876432G>A | CA421138577 | NTRK1 | c.1485G>A (p.Gln495=) c.*257G>A (n.*257G>A) c.1665G>A (p.Gln555=) c.1656G>A (p.Gln552=) c.1647G>A (p.Gln549=) c.1557G>A (p.Gln519=) n.2118G>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156876432G>C | CA342938450 | NTRK1 | c.1485G>C (p.Gln495His) c.*257G>C (n.*257G>C) c.1665G>C (p.Gln555His) c.1656G>C (p.Gln552His) c.1647G>C (p.Gln549His) c.1557G>C (p.Gln519His) n.2118G>C | dbSNP |
| 1 | g.156876432G>T | CA342938451 | NTRK1 | c.1485G>T (p.Gln495His) c.*257G>T (n.*257G>T) c.1665G>T (p.Gln555His) c.1656G>T (p.Gln552His) c.1647G>T (p.Gln549His) c.1557G>T (p.Gln519His) n.2118G>T | dbSNP |
| 1 | g.156876433G>A | CA342938453 | NTRK1 | c.1486G>A (p.Asp496Asn) c.*258G>A (n.*258G>A) c.1666G>A (p.Asp556Asn) c.1657G>A (p.Asp553Asn) c.1648G>A (p.Asp550Asn) c.1558G>A (p.Asp520Asn) n.2119G>A | dbSNP |
| 1 | g.156876433G>C | CA342938454 | NTRK1 | c.1486G>C (p.Asp496His) c.*258G>C (n.*258G>C) c.1666G>C (p.Asp556His) c.1657G>C (p.Asp553His) c.1648G>C (p.Asp550His) c.1558G>C (p.Asp520His) n.2119G>C | dbSNP |
| 1 | g.156876433G>T | CA342938452 | NTRK1 | c.1486G>T (p.Asp496Tyr) c.*258G>T (n.*258G>T) c.1666G>T (p.Asp556Tyr) c.1657G>T (p.Asp553Tyr) c.1648G>T (p.Asp550Tyr) c.1558G>T (p.Asp520Tyr) n.2119G>T | dbSNP |
| 1 | g.156876434A>C | CA342938456 | NTRK1 | c.1487A>C (p.Asp496Ala) c.*259A>C (n.*259A>C) c.1667A>C (p.Asp556Ala) c.1658A>C (p.Asp553Ala) c.1649A>C (p.Asp550Ala) c.1559A>C (p.Asp520Ala) n.2120A>C | dbSNP gnomAD v4 |
| 1 | g.156876434A>G | CA342938455 | NTRK1 | c.1487A>G (p.Asp496Gly) c.*259A>G (n.*259A>G) c.1667A>G (p.Asp556Gly) c.1658A>G (p.Asp553Gly) c.1649A>G (p.Asp550Gly) c.1559A>G (p.Asp520Gly) n.2120A>G | dbSNP |
| 1 | g.156876434A>T | CA342938457 | NTRK1 | c.1487A>T (p.Asp496Val) c.*259A>T (n.*259A>T) c.1667A>T (p.Asp556Val) c.1658A>T (p.Asp553Val) c.1649A>T (p.Asp550Val) c.1559A>T (p.Asp520Val) n.2120A>T | dbSNP |
| 1 | g.156876435C>A | CA342938458 | NTRK1 | c.1488C>A (p.Asp496Glu) c.*260C>A (n.*260C>A) c.1668C>A (p.Asp556Glu) c.1659C>A (p.Asp553Glu) c.1650C>A (p.Asp550Glu) c.1560C>A (p.Asp520Glu) n.2121C>A | dbSNP |
| 1 | g.156876435C>G | CA342938459 | NTRK1 | c.1488C>G (p.Asp496Glu) c.*260C>G (n.*260C>G) c.1668C>G (p.Asp556Glu) c.1659C>G (p.Asp553Glu) c.1650C>G (p.Asp550Glu) c.1560C>G (p.Asp520Glu) n.2121C>G | dbSNP |
| 1 | g.156876435C>T | CA421138591 | NTRK1 | c.1488C>T (p.Asp496=) c.*260C>T (n.*260C>T) c.1668C>T (p.Asp556=) c.1659C>T (p.Asp553=) c.1650C>T (p.Asp550=) c.1560C>T (p.Asp520=) n.2121C>T | ClinVar dbSNP |
| 1 | g.156876436T>A | CA342938460 | NTRK1 | c.1489T>A (p.Phe497Ile) c.*261T>A (n.*261T>A) c.1669T>A (p.Phe557Ile) c.1660T>A (p.Phe554Ile) c.1651T>A (p.Phe551Ile) c.1561T>A (p.Phe521Ile) n.2122T>A | dbSNP |
| 1 | g.156876436T>C | CA342938461 | NTRK1 | c.1489T>C (p.Phe497Leu) c.*261T>C (n.*261T>C) c.1669T>C (p.Phe557Leu) c.1660T>C (p.Phe554Leu) c.1651T>C (p.Phe551Leu) c.1561T>C (p.Phe521Leu) n.2122T>C | dbSNP |
| 1 | g.156876436T>G | CA342938462 | NTRK1 | c.1489T>G (p.Phe497Val) c.*261T>G (n.*261T>G) c.1669T>G (p.Phe557Val) c.1660T>G (p.Phe554Val) c.1651T>G (p.Phe551Val) c.1561T>G (p.Phe521Val) n.2122T>G | |
| 1 | g.156876437T>A | CA342938463 | NTRK1 | c.1490T>A (p.Phe497Tyr) c.*262T>A (n.*262T>A) c.1670T>A (p.Phe557Tyr) c.1661T>A (p.Phe554Tyr) c.1652T>A (p.Phe551Tyr) c.1562T>A (p.Phe521Tyr) n.2123T>A | |
| 1 | g.156876437T>C | CA342938464 | NTRK1 | c.1490T>C (p.Phe497Ser) c.*262T>C (n.*262T>C) c.1670T>C (p.Phe557Ser) c.1661T>C (p.Phe554Ser) c.1652T>C (p.Phe551Ser) c.1562T>C (p.Phe521Ser) n.2123T>C | |
| 1 | g.156876437T>G | CA342938465 | NTRK1 | c.1490T>G (p.Phe497Cys) c.*262T>G (n.*262T>G) c.1670T>G (p.Phe557Cys) c.1661T>G (p.Phe554Cys) c.1652T>G (p.Phe551Cys) c.1562T>G (p.Phe521Cys) n.2123T>G | |
| 1 | g.156876437_156876438delinsAT | CA645518200 | NTRK1 | c.1490_1491delinsAT (p.Phe497Tyr) c.*262_*263delinsAT (n.*262_*263delinsAT) c.1670_1671delinsAT (p.Phe557Tyr) c.1661_1662delinsAT (p.Phe554Tyr) c.1652_1653delinsAT (p.Phe551Tyr) c.1562_1563delinsAT (p.Phe521Tyr) n.2123_2124delinsAT | COSMIC COSMIC |
| 1 | g.156876438C>A | CA342938466 | NTRK1 | c.1491C>A (p.Phe497Leu) c.*263C>A (n.*263C>A) c.1671C>A (p.Phe557Leu) c.1662C>A (p.Phe554Leu) c.1653C>A (p.Phe551Leu) c.1563C>A (p.Phe521Leu) n.2124C>A | |
| 1 | g.156876438C>G | CA342938467 | NTRK1 | c.1491C>G (p.Phe497Leu) c.*263C>G (n.*263C>G) c.1671C>G (p.Phe557Leu) c.1662C>G (p.Phe554Leu) c.1653C>G (p.Phe551Leu) c.1563C>G (p.Phe521Leu) n.2124C>G | dbSNP |
| 1 | g.156876438C>T | CA421138606 | NTRK1 | c.1491C>T (p.Phe497=) c.*263C>T (n.*263C>T) c.1671C>T (p.Phe557=) c.1662C>T (p.Phe554=) c.1653C>T (p.Phe551=) c.1563C>T (p.Phe521=) n.2124C>T | ClinVar dbSNP |
| 1 | g.156876439del | CA2648464067 | NTRK1 | c.1492del (p.Gln498SerfsTer?) c.*264del (n.*264del) c.1672del (p.Gln558SerfsTer?) c.1663del (p.Gln555SerfsTer?) c.1654del (p.Gln552SerfsTer?) c.1564del (p.Gln522SerfsTer?) n.2125del | gnomAD v4 |
| 1 | g.156876439C>A | CA342938468 | NTRK1 | c.1492C>A (p.Gln498Lys) c.*264C>A (n.*264C>A) c.1672C>A (p.Gln558Lys) c.1663C>A (p.Gln555Lys) c.1654C>A (p.Gln552Lys) c.1564C>A (p.Gln522Lys) n.2125C>A | |
| 1 | g.156876439C>G | CA342938469 | NTRK1 | c.1492C>G (p.Gln498Glu) c.*264C>G (n.*264C>G) c.1672C>G (p.Gln558Glu) c.1663C>G (p.Gln555Glu) c.1654C>G (p.Gln552Glu) c.1564C>G (p.Gln522Glu) n.2125C>G | dbSNP |
| 1 | g.156876439C>T | CA342938470 | NTRK1 | c.1492C>T (p.Gln498Ter) c.*264C>T (n.*264C>T) c.1672C>T (p.Gln558Ter) c.1663C>T (p.Gln555Ter) c.1654C>T (p.Gln552Ter) c.1564C>T (p.Gln522Ter) n.2125C>T | |
| 1 | g.156876440A= | CA1200786096 | NTRK1 | c.1493A= (p.Gln498=) c.*265A= (n.*265A=) c.1673A= (p.Gln558=) c.1664A= (p.Gln555=) c.1655A= (p.Gln552=) c.1565A= (p.Gln522=) n.2126A= | |
| 1 | g.156876440A>C | CA342938473 | NTRK1 | c.1493A>C (p.Gln498Pro) c.*265A>C (n.*265A>C) c.1673A>C (p.Gln558Pro) c.1664A>C (p.Gln555Pro) c.1655A>C (p.Gln552Pro) c.1565A>C (p.Gln522Pro) n.2126A>C | |
| 1 | g.156876440A>G | CA342938472 | NTRK1 | c.1493A>G (p.Gln498Arg) c.*265A>G (n.*265A>G) c.1673A>G (p.Gln558Arg) c.1664A>G (p.Gln555Arg) c.1655A>G (p.Gln552Arg) c.1565A>G (p.Gln522Arg) n.2126A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876440A>T | CA342938471 | NTRK1 | c.1493A>T (p.Gln498Leu) c.*265A>T (n.*265A>T) c.1673A>T (p.Gln558Leu) c.1664A>T (p.Gln555Leu) c.1655A>T (p.Gln552Leu) c.1565A>T (p.Gln522Leu) n.2126A>T | dbSNP |
| 1 | g.156876441G>A | CA1169435 | NTRK1 | c.1494G>A (p.Gln498=) c.*266G>A (n.*266G>A) c.1674G>A (p.Gln558=) c.1665G>A (p.Gln555=) c.1656G>A (p.Gln552=) c.1566G>A (p.Gln522=) n.2127G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876441G>C | CA1169436 | NTRK1 | c.1494G>C (p.Gln498His) c.*266G>C (n.*266G>C) c.1674G>C (p.Gln558His) c.1665G>C (p.Gln555His) c.1656G>C (p.Gln552His) c.1566G>C (p.Gln522His) n.2127G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876441G= | CA1139773135 | NTRK1 | c.1494G= (p.Gln498=) c.*266G= (n.*266G=) c.1674G= (p.Gln558=) c.1665G= (p.Gln555=) c.1656G= (p.Gln552=) c.1566G= (p.Gln522=) n.2127G= | |
| 1 | g.156876441G>T | CA342938474 | NTRK1 | c.1494G>T (p.Gln498His) c.*266G>T (n.*266G>T) c.1674G>T (p.Gln558His) c.1665G>T (p.Gln555His) c.1656G>T (p.Gln552His) c.1566G>T (p.Gln522His) n.2127G>T | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876442C>A | CA342938475 | NTRK1 | c.1495C>A (p.Arg499Ser) c.*267C>A (n.*267C>A) c.1675C>A (p.Arg559Ser) c.1666C>A (p.Arg556Ser) c.1657C>A (p.Arg553Ser) c.1567C>A (p.Arg523Ser) n.2128C>A | dbSNP |
| 1 | g.156876442C= | CA1200786097 | NTRK1 | c.1495C= (p.Arg499=) c.*267C= (n.*267C=) c.1675C= (p.Arg559=) c.1666C= (p.Arg556=) c.1657C= (p.Arg553=) c.1567C= (p.Arg523=) n.2128C= | |
| 1 | g.156876442C>G | CA342938476 | NTRK1 | c.1495C>G (p.Arg499Gly) c.*267C>G (n.*267C>G) c.1675C>G (p.Arg559Gly) c.1666C>G (p.Arg556Gly) c.1657C>G (p.Arg553Gly) c.1567C>G (p.Arg523Gly) n.2128C>G | ClinVar dbSNP |
| 1 | g.156876442C>T | CA1169437 | NTRK1 | c.1495C>T (p.Arg499Cys) c.*267C>T (n.*267C>T) c.1675C>T (p.Arg559Cys) c.1666C>T (p.Arg556Cys) c.1657C>T (p.Arg553Cys) c.1567C>T (p.Arg523Cys) n.2128C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876443G>A | CA1169438 | NTRK1 | c.1496G>A (p.Arg499His) c.*268G>A (n.*268G>A) c.1676G>A (p.Arg559His) c.1667G>A (p.Arg556His) c.1658G>A (p.Arg553His) c.1568G>A (p.Arg523His) n.2129G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876443G>C | CA342938477 | NTRK1 | c.1496G>C (p.Arg499Pro) c.*268G>C (n.*268G>C) c.1676G>C (p.Arg559Pro) c.1667G>C (p.Arg556Pro) c.1658G>C (p.Arg553Pro) c.1568G>C (p.Arg523Pro) n.2129G>C | dbSNP |
| 1 | g.156876443G= | CA1143490812 | NTRK1 | c.1496G= (p.Arg499=) c.*268G= (n.*268G=) c.1676G= (p.Arg559=) c.1667G= (p.Arg556=) c.1658G= (p.Arg553=) c.1568G= (p.Arg523=) n.2129G= | |
| 1 | g.156876443G>T | CA342938478 | NTRK1 | c.1496G>T (p.Arg499Leu) c.*268G>T (n.*268G>T) c.1676G>T (p.Arg559Leu) c.1667G>T (p.Arg556Leu) c.1658G>T (p.Arg553Leu) c.1568G>T (p.Arg523Leu) n.2129G>T | |
| 1 | g.156876444T>A | CA421138630 | NTRK1 | c.1497T>A (p.Arg499=) c.*269T>A (n.*269T>A) c.1677T>A (p.Arg559=) c.1668T>A (p.Arg556=) c.1659T>A (p.Arg553=) c.1569T>A (p.Arg523=) n.2130T>A | dbSNP |
| 1 | g.156876444T>C | CA421138633 | NTRK1 | c.1497T>C (p.Arg499=) c.*269T>C (n.*269T>C) c.1677T>C (p.Arg559=) c.1668T>C (p.Arg556=) c.1659T>C (p.Arg553=) c.1569T>C (p.Arg523=) n.2130T>C | dbSNP |
| 1 | g.156876444T>G | CA421138635 | NTRK1 | c.1497T>G (p.Arg499=) c.*269T>G (n.*269T>G) c.1677T>G (p.Arg559=) c.1668T>G (p.Arg556=) c.1659T>G (p.Arg553=) c.1569T>G (p.Arg523=) n.2130T>G | dbSNP |
| 1 | g.156876444T= | CA1200786098 | NTRK1 | c.1497T= (p.Arg499=) c.*269T= (n.*269T=) c.1677T= (p.Arg559=) c.1668T= (p.Arg556=) c.1659T= (p.Arg553=) c.1569T= (p.Arg523=) n.2130T= | |
| 1 | g.156876445G>A | CA31118766 | NTRK1 | c.1498G>A (p.Glu500Lys) c.*270G>A (n.*270G>A) c.1678G>A (p.Glu560Lys) c.1669G>A (p.Glu557Lys) c.1660G>A (p.Glu554Lys) c.1570G>A (p.Glu524Lys) n.2131G>A | dbSNP |
| 1 | g.156876445G>C | CA342938479 | NTRK1 | c.1498G>C (p.Glu500Gln) c.*270G>C (n.*270G>C) c.1678G>C (p.Glu560Gln) c.1669G>C (p.Glu557Gln) c.1660G>C (p.Glu554Gln) c.1570G>C (p.Glu524Gln) n.2131G>C | dbSNP |
| 1 | g.156876445G= | CA1140614573 | NTRK1 | c.1498G= (p.Glu500=) c.*270G= (n.*270G=) c.1678G= (p.Glu560=) c.1669G= (p.Glu557=) c.1660G= (p.Glu554=) c.1570G= (p.Glu524=) n.2131G= | |
| 1 | g.156876445G>T | CA342938480 | NTRK1 | c.1498G>T (p.Glu500Ter) c.*270G>T (n.*270G>T) c.1678G>T (p.Glu560Ter) c.1669G>T (p.Glu557Ter) c.1660G>T (p.Glu554Ter) c.1570G>T (p.Glu524Ter) n.2131G>T | dbSNP |
| 1 | g.156876446A>C | CA342938483 | NTRK1 | c.1499A>C (p.Glu500Ala) c.*271A>C (n.*271A>C) c.1679A>C (p.Glu560Ala) c.1670A>C (p.Glu557Ala) c.1661A>C (p.Glu554Ala) c.1571A>C (p.Glu524Ala) n.2132A>C | |
| 1 | g.156876446A>G | CA342938482 | NTRK1 | c.1499A>G (p.Glu500Gly) c.*271A>G (n.*271A>G) c.1679A>G (p.Glu560Gly) c.1670A>G (p.Glu557Gly) c.1661A>G (p.Glu554Gly) c.1571A>G (p.Glu524Gly) n.2132A>G | |
| 1 | g.156876446A>T | CA342938481 | NTRK1 | c.1499A>T (p.Glu500Val) c.*271A>T (n.*271A>T) c.1679A>T (p.Glu560Val) c.1670A>T (p.Glu557Val) c.1661A>T (p.Glu554Val) c.1571A>T (p.Glu524Val) n.2132A>T | |
| 1 | g.156876447G>A | CA421138641 | NTRK1 | c.1500G>A (p.Glu500=) c.*272G>A (n.*272G>A) c.1680G>A (p.Glu560=) c.1671G>A (p.Glu557=) c.1662G>A (p.Glu554=) c.1572G>A (p.Glu524=) n.2133G>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156876447G>C | CA342938484 | NTRK1 | c.1500G>C (p.Glu500Asp) c.*272G>C (n.*272G>C) c.1680G>C (p.Glu560Asp) c.1671G>C (p.Glu557Asp) c.1662G>C (p.Glu554Asp) c.1572G>C (p.Glu524Asp) n.2133G>C | dbSNP |
| 1 | g.156876447G>T | CA342938485 | NTRK1 | c.1500G>T (p.Glu500Asp) c.*272G>T (n.*272G>T) c.1680G>T (p.Glu560Asp) c.1671G>T (p.Glu557Asp) c.1662G>T (p.Glu554Asp) c.1572G>T (p.Glu524Asp) n.2133G>T | dbSNP |
| 1 | g.156876448G>A | CA342938486 | NTRK1 | c.1501G>A (p.Ala501Thr) c.*273G>A (n.*273G>A) c.1681G>A (p.Ala561Thr) c.1672G>A (p.Ala558Thr) c.1663G>A (p.Ala555Thr) c.1573G>A (p.Ala525Thr) n.2134G>A | dbSNP gnomAD v2 |
| 1 | g.156876448G>C | CA342938487 | NTRK1 | c.1501G>C (p.Ala501Pro) c.*273G>C (n.*273G>C) c.1681G>C (p.Ala561Pro) c.1672G>C (p.Ala558Pro) c.1663G>C (p.Ala555Pro) c.1573G>C (p.Ala525Pro) n.2134G>C | dbSNP |
| 1 | g.156876448G= | CA1200786099 | NTRK1 | c.1501G= (p.Ala501=) c.*273G= (n.*273G=) c.1681G= (p.Ala561=) c.1672G= (p.Ala558=) c.1663G= (p.Ala555=) c.1573G= (p.Ala525=) n.2134G= | |
| 1 | g.156876448G>T | CA342938488 | NTRK1 | c.1501G>T (p.Ala501Ser) c.*273G>T (n.*273G>T) c.1681G>T (p.Ala561Ser) c.1672G>T (p.Ala558Ser) c.1663G>T (p.Ala555Ser) c.1573G>T (p.Ala525Ser) n.2134G>T | |
| 1 | g.156876449C>A | CA342938489 | NTRK1 | c.1502C>A (p.Ala501Asp) c.*274C>A (n.*274C>A) c.1682C>A (p.Ala561Asp) c.1673C>A (p.Ala558Asp) c.1664C>A (p.Ala555Asp) c.1574C>A (p.Ala525Asp) n.2135C>A | dbSNP |
| 1 | g.156876449C>G | CA342938490 | NTRK1 | c.1502C>G (p.Ala501Gly) c.*274C>G (n.*274C>G) c.1682C>G (p.Ala561Gly) c.1673C>G (p.Ala558Gly) c.1664C>G (p.Ala555Gly) c.1574C>G (p.Ala525Gly) n.2135C>G | dbSNP |
| 1 | g.156876449C>T | CA342938491 | NTRK1 | c.1502C>T (p.Ala501Val) c.*274C>T (n.*274C>T) c.1682C>T (p.Ala561Val) c.1673C>T (p.Ala558Val) c.1664C>T (p.Ala555Val) c.1574C>T (p.Ala525Val) n.2135C>T | |
| 1 | g.156876450T>A | CA421138646 | NTRK1 | c.1503T>A (p.Ala501=) c.*275T>A (n.*275T>A) c.1683T>A (p.Ala561=) c.1674T>A (p.Ala558=) c.1665T>A (p.Ala555=) c.1575T>A (p.Ala525=) n.2136T>A | |
| 1 | g.156876450T>C | CA421138648 | NTRK1 | c.1503T>C (p.Ala501=) c.*275T>C (n.*275T>C) c.1683T>C (p.Ala561=) c.1674T>C (p.Ala558=) c.1665T>C (p.Ala555=) c.1575T>C (p.Ala525=) n.2136T>C | |
| 1 | g.156876450T>G | CA421138649 | NTRK1 | c.1503T>G (p.Ala501=) c.*275T>G (n.*275T>G) c.1683T>G (p.Ala561=) c.1674T>G (p.Ala558=) c.1665T>G (p.Ala555=) c.1575T>G (p.Ala525=) n.2136T>G | gnomAD v4 |
| 1 | g.156876451G>A | CA342938492 | NTRK1 | c.1504G>A (p.Glu502Lys) c.*276G>A (n.*276G>A) c.1684G>A (p.Glu562Lys) c.1675G>A (p.Glu559Lys) c.1666G>A (p.Glu556Lys) c.1576G>A (p.Glu526Lys) n.2137G>A | dbSNP |
| 1 | g.156876451G>C | CA342938493 | NTRK1 | c.1504G>C (p.Glu502Gln) c.*276G>C (n.*276G>C) c.1684G>C (p.Glu562Gln) c.1675G>C (p.Glu559Gln) c.1666G>C (p.Glu556Gln) c.1576G>C (p.Glu526Gln) n.2137G>C | dbSNP |
| 1 | g.156876451G>T | CA342938494 | NTRK1 | c.1504G>T (p.Glu502Ter) c.*276G>T (n.*276G>T) c.1684G>T (p.Glu562Ter) c.1675G>T (p.Glu559Ter) c.1666G>T (p.Glu556Ter) c.1576G>T (p.Glu526Ter) n.2137G>T | dbSNP |
| 1 | g.156876452A= | CA1200786100 | NTRK1 | c.1505A= (p.Glu502=) c.*277A= (n.*277A=) c.1685A= (p.Glu562=) c.1676A= (p.Glu559=) c.1667A= (p.Glu556=) c.1577A= (p.Glu526=) n.2138A= | |
| 1 | g.156876452A>C | CA342938495 | NTRK1 | c.1505A>C (p.Glu502Ala) c.*277A>C (n.*277A>C) c.1685A>C (p.Glu562Ala) c.1676A>C (p.Glu559Ala) c.1667A>C (p.Glu556Ala) c.1577A>C (p.Glu526Ala) n.2138A>C | dbSNP |
| 1 | g.156876452A>G | CA342938496 | NTRK1 | c.1505A>G (p.Glu502Gly) c.*277A>G (n.*277A>G) c.1685A>G (p.Glu562Gly) c.1676A>G (p.Glu559Gly) c.1667A>G (p.Glu556Gly) c.1577A>G (p.Glu526Gly) n.2138A>G | dbSNP |
| 1 | g.156876452A>T | CA342938497 | NTRK1 | c.1505A>T (p.Glu502Val) c.*277A>T (n.*277A>T) c.1685A>T (p.Glu562Val) c.1676A>T (p.Glu559Val) c.1667A>T (p.Glu556Val) c.1577A>T (p.Glu526Val) n.2138A>T | dbSNP |
| 1 | g.156876452_156876454del | CA2648464100 | NTRK1 | c.1505_1507del (p.Glu502_Leu503delinsVal) c.*277_*279del (n.*277_*279del) c.1685_1687del (p.Glu562_Leu563delinsVal) c.1676_1678del (p.Glu559_Leu560delinsVal) c.1667_1669del (p.Glu556_Leu557delinsVal) c.1577_1579del (p.Glu526_Leu527delinsVal) n.2138_2140del | gnomAD v4 |
| 1 | g.156876453G>A | CA421138655 | NTRK1 | c.1506G>A (p.Glu502=) c.*278G>A (n.*278G>A) c.1686G>A (p.Glu562=) c.1677G>A (p.Glu559=) c.1668G>A (p.Glu556=) c.1578G>A (p.Glu526=) n.2139G>A | dbSNP gnomAD v4 |
| 1 | g.156876453G>C | CA342938498 | NTRK1 | c.1506G>C (p.Glu502Asp) c.*278G>C (n.*278G>C) c.1686G>C (p.Glu562Asp) c.1677G>C (p.Glu559Asp) c.1668G>C (p.Glu556Asp) c.1578G>C (p.Glu526Asp) n.2139G>C | dbSNP |
| 1 | g.156876453G>T | CA342938499 | NTRK1 | c.1506G>T (p.Glu502Asp) c.*278G>T (n.*278G>T) c.1686G>T (p.Glu562Asp) c.1677G>T (p.Glu559Asp) c.1668G>T (p.Glu556Asp) c.1578G>T (p.Glu526Asp) n.2139G>T | dbSNP |
| 1 | g.156876454C>A | CA342938500 | NTRK1 | c.1507C>A (p.Leu503Met) c.*279C>A (n.*279C>A) c.1687C>A (p.Leu563Met) c.1678C>A (p.Leu560Met) c.1669C>A (p.Leu557Met) c.1579C>A (p.Leu527Met) n.2140C>A | dbSNP |
| 1 | g.156876454C>G | CA342938501 | NTRK1 | c.1507C>G (p.Leu503Val) c.*279C>G (n.*279C>G) c.1687C>G (p.Leu563Val) c.1678C>G (p.Leu560Val) c.1669C>G (p.Leu557Val) c.1579C>G (p.Leu527Val) n.2140C>G | ClinVar dbSNP |
| 1 | g.156876454C>T | CA421138660 | NTRK1 | c.1507C>T (p.Leu503=) c.*279C>T (n.*279C>T) c.1687C>T (p.Leu563=) c.1678C>T (p.Leu560=) c.1669C>T (p.Leu557=) c.1579C>T (p.Leu527=) n.2140C>T | dbSNP |
| 1 | g.156876455T>A | CA342938502 | NTRK1 | c.1508T>A (p.Leu503Gln) c.*280T>A (n.*280T>A) c.1688T>A (p.Leu563Gln) c.1679T>A (p.Leu560Gln) c.1670T>A (p.Leu557Gln) c.1580T>A (p.Leu527Gln) n.2141T>A | dbSNP |
| 1 | g.156876455T>C | CA342938503 | NTRK1 | c.1508T>C (p.Leu503Pro) c.*280T>C (n.*280T>C) c.1688T>C (p.Leu563Pro) c.1679T>C (p.Leu560Pro) c.1670T>C (p.Leu557Pro) c.1580T>C (p.Leu527Pro) n.2141T>C | dbSNP |
| 1 | g.156876455T>G | CA342938504 | NTRK1 | c.1508T>G (p.Leu503Arg) c.*280T>G (n.*280T>G) c.1688T>G (p.Leu563Arg) c.1679T>G (p.Leu560Arg) c.1670T>G (p.Leu557Arg) c.1580T>G (p.Leu527Arg) n.2141T>G | dbSNP |
| 1 | g.156876456G>A | CA421138669 | NTRK1 | c.1509G>A (p.Leu503=) c.*281G>A (n.*281G>A) c.1689G>A (p.Leu563=) c.1680G>A (p.Leu560=) c.1671G>A (p.Leu557=) c.1581G>A (p.Leu527=) n.2142G>A | dbSNP |
| 1 | g.156876456G>C | CA421138671 | NTRK1 | c.1509G>C (p.Leu503=) c.*281G>C (n.*281G>C) c.1689G>C (p.Leu563=) c.1680G>C (p.Leu560=) c.1671G>C (p.Leu557=) c.1581G>C (p.Leu527=) n.2142G>C | dbSNP |
| 1 | g.156876456G>T | CA421138667 | NTRK1 | c.1509G>T (p.Leu503=) c.*281G>T (n.*281G>T) c.1689G>T (p.Leu563=) c.1680G>T (p.Leu560=) c.1671G>T (p.Leu557=) c.1581G>T (p.Leu527=) n.2142G>T | dbSNP gnomAD v4 |
| 1 | g.156876457C>A | CA342938505 | NTRK1 | c.1510C>A (p.Leu504Ile) c.*282C>A (n.*282C>A) c.1690C>A (p.Leu564Ile) c.1681C>A (p.Leu561Ile) c.1672C>A (p.Leu558Ile) c.1582C>A (p.Leu528Ile) n.2143C>A | dbSNP |
| 1 | g.156876457C= | CA1200786101 | NTRK1 | c.1510C= (p.Leu504=) c.*282C= (n.*282C=) c.1690C= (p.Leu564=) c.1681C= (p.Leu561=) c.1672C= (p.Leu558=) c.1582C= (p.Leu528=) n.2143C= | |
| 1 | g.156876457C>G | CA342938506 | NTRK1 | c.1510C>G (p.Leu504Val) c.*282C>G (n.*282C>G) c.1690C>G (p.Leu564Val) c.1681C>G (p.Leu561Val) c.1672C>G (p.Leu558Val) c.1582C>G (p.Leu528Val) n.2143C>G | dbSNP |
| 1 | g.156876457C>T | CA342938507 | NTRK1 | c.1510C>T (p.Leu504Phe) c.*282C>T (n.*282C>T) c.1690C>T (p.Leu564Phe) c.1681C>T (p.Leu561Phe) c.1672C>T (p.Leu558Phe) c.1582C>T (p.Leu528Phe) n.2143C>T | ClinVar dbSNP |
| 1 | g.156876458T>A | CA342938508 | NTRK1 | c.1511T>A (p.Leu504His) c.*283T>A (n.*283T>A) c.1691T>A (p.Leu564His) c.1682T>A (p.Leu561His) c.1673T>A (p.Leu558His) c.1583T>A (p.Leu528His) n.2144T>A | |
| 1 | g.156876458T>C | CA342938509 | NTRK1 | c.1511T>C (p.Leu504Pro) c.*283T>C (n.*283T>C) c.1691T>C (p.Leu564Pro) c.1682T>C (p.Leu561Pro) c.1673T>C (p.Leu558Pro) c.1583T>C (p.Leu528Pro) n.2144T>C | |
| 1 | g.156876458T>G | CA342938510 | NTRK1 | c.1511T>G (p.Leu504Arg) c.*283T>G (n.*283T>G) c.1691T>G (p.Leu564Arg) c.1682T>G (p.Leu561Arg) c.1673T>G (p.Leu558Arg) c.1583T>G (p.Leu528Arg) n.2144T>G | |
| 1 | g.156876459C>A | CA421138683 | NTRK1 | c.1512C>A (p.Leu504=) c.*284C>A (n.*284C>A) c.1692C>A (p.Leu564=) c.1683C>A (p.Leu561=) c.1674C>A (p.Leu558=) c.1584C>A (p.Leu528=) n.2145C>A | dbSNP |
| 1 | g.156876459C= | CA1200786102 | NTRK1 | c.1512C= (p.Leu504=) c.*284C= (n.*284C=) c.1692C= (p.Leu564=) c.1683C= (p.Leu561=) c.1674C= (p.Leu558=) c.1584C= (p.Leu528=) n.2145C= | |
| 1 | g.156876459C>G | CA421138681 | NTRK1 | c.1512C>G (p.Leu504=) c.*284C>G (n.*284C>G) c.1692C>G (p.Leu564=) c.1683C>G (p.Leu561=) c.1674C>G (p.Leu558=) c.1584C>G (p.Leu528=) n.2145C>G | dbSNP |
| 1 | g.156876459C>T | CA421138679 | NTRK1 | c.1512C>T (p.Leu504=) c.*284C>T (n.*284C>T) c.1692C>T (p.Leu564=) c.1683C>T (p.Leu561=) c.1674C>T (p.Leu558=) c.1584C>T (p.Leu528=) n.2145C>T | dbSNP gnomAD v4 |
| 1 | g.156876460A>C | CA342938513 | NTRK1 | c.1513A>C (p.Thr505Pro) c.*285A>C (n.*285A>C) c.1693A>C (p.Thr565Pro) c.1684A>C (p.Thr562Pro) c.1675A>C (p.Thr559Pro) c.1585A>C (p.Thr529Pro) n.2146A>C | dbSNP |
| 1 | g.156876460A>G | CA342938512 | NTRK1 | c.1513A>G (p.Thr505Ala) c.*285A>G (n.*285A>G) c.1693A>G (p.Thr565Ala) c.1684A>G (p.Thr562Ala) c.1675A>G (p.Thr559Ala) c.1585A>G (p.Thr529Ala) n.2146A>G | |
| 1 | g.156876460A>T | CA342938511 | NTRK1 | c.1513A>T (p.Thr505Ser) c.*285A>T (n.*285A>T) c.1693A>T (p.Thr565Ser) c.1684A>T (p.Thr562Ser) c.1675A>T (p.Thr559Ser) c.1585A>T (p.Thr529Ser) n.2146A>T | dbSNP |
| 1 | g.156876461C>A | CA342938514 | NTRK1 | c.1514C>A (p.Thr505Asn) c.*286C>A (n.*286C>A) c.1694C>A (p.Thr565Asn) c.1685C>A (p.Thr562Asn) c.1676C>A (p.Thr559Asn) c.1586C>A (p.Thr529Asn) n.2147C>A | |
| 1 | g.156876461C= | CA1200786103 | NTRK1 | c.1514C= (p.Thr505=) c.*286C= (n.*286C=) c.1694C= (p.Thr565=) c.1685C= (p.Thr562=) c.1676C= (p.Thr559=) c.1586C= (p.Thr529=) n.2147C= | |
| 1 | g.156876461C>G | CA342938515 | NTRK1 | c.1514C>G (p.Thr505Ser) c.*286C>G (n.*286C>G) c.1694C>G (p.Thr565Ser) c.1685C>G (p.Thr562Ser) c.1676C>G (p.Thr559Ser) c.1586C>G (p.Thr529Ser) n.2147C>G | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876461C>T | CA342938516 | NTRK1 | c.1514C>T (p.Thr505Ile) c.*286C>T (n.*286C>T) c.1694C>T (p.Thr565Ile) c.1685C>T (p.Thr562Ile) c.1676C>T (p.Thr559Ile) c.1586C>T (p.Thr529Ile) n.2147C>T | dbSNP |
| 1 | g.156876462C>A | CA421138692 | NTRK1 | c.1515C>A (p.Thr505=) c.*287C>A (n.*287C>A) c.1695C>A (p.Thr565=) c.1686C>A (p.Thr562=) c.1677C>A (p.Thr559=) c.1587C>A (p.Thr529=) n.2148C>A | |
| 1 | g.156876462C= | CA1200786104 | NTRK1 | c.1515C= (p.Thr505=) c.*287C= (n.*287C=) c.1695C= (p.Thr565=) c.1686C= (p.Thr562=) c.1677C= (p.Thr559=) c.1587C= (p.Thr529=) n.2148C= | |
| 1 | g.156876462C>G | CA421138693 | NTRK1 | c.1515C>G (p.Thr505=) c.*287C>G (n.*287C>G) c.1695C>G (p.Thr565=) c.1686C>G (p.Thr562=) c.1677C>G (p.Thr559=) c.1587C>G (p.Thr529=) n.2148C>G | dbSNP |
| 1 | g.156876462C>T | CA31118767 | NTRK1 | c.1515C>T (p.Thr505=) c.*287C>T (n.*287C>T) c.1695C>T (p.Thr565=) c.1686C>T (p.Thr562=) c.1677C>T (p.Thr559=) c.1587C>T (p.Thr529=) n.2148C>T | ClinVar dbSNP |
| 1 | g.156876463A= | CA1200786105 | NTRK1 | c.1516A= (p.Met506=) c.*288A= (n.*288A=) c.1696A= (p.Met566=) c.1687A= (p.Met563=) c.1678A= (p.Met560=) c.1588A= (p.Met530=) n.2149A= | |
| 1 | g.156876463A>C | CA342938517 | NTRK1 | c.1516A>C (p.Met506Leu) c.*288A>C (n.*288A>C) c.1696A>C (p.Met566Leu) c.1687A>C (p.Met563Leu) c.1678A>C (p.Met560Leu) c.1588A>C (p.Met530Leu) n.2149A>C | dbSNP |
| 1 | g.156876463A>G | CA342938518 | NTRK1 | c.1516A>G (p.Met506Val) c.*288A>G (n.*288A>G) c.1696A>G (p.Met566Val) c.1687A>G (p.Met563Val) c.1678A>G (p.Met560Val) c.1588A>G (p.Met530Val) n.2149A>G | gnomAD v4 |
| 1 | g.156876463A>T | CA342938519 | NTRK1 | c.1516A>T (p.Met506Leu) c.*288A>T (n.*288A>T) c.1696A>T (p.Met566Leu) c.1687A>T (p.Met563Leu) c.1678A>T (p.Met560Leu) c.1588A>T (p.Met530Leu) n.2149A>T | dbSNP |
| 1 | g.156876464T>A | CA1169440 | NTRK1 | c.1517T>A (p.Met506Lys) c.*289T>A (n.*289T>A) c.1697T>A (p.Met566Lys) c.1688T>A (p.Met563Lys) c.1679T>A (p.Met560Lys) c.1589T>A (p.Met530Lys) n.2150T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876464T>C | CA1169439 | NTRK1 | c.1517T>C (p.Met506Thr) c.*289T>C (n.*289T>C) c.1697T>C (p.Met566Thr) c.1688T>C (p.Met563Thr) c.1679T>C (p.Met560Thr) c.1589T>C (p.Met530Thr) n.2150T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876464T>G | CA342938520 | NTRK1 | c.1517T>G (p.Met506Arg) c.*289T>G (n.*289T>G) c.1697T>G (p.Met566Arg) c.1688T>G (p.Met563Arg) c.1679T>G (p.Met560Arg) c.1589T>G (p.Met530Arg) n.2150T>G | dbSNP |
| 1 | g.156876464T= | CA1140625675 | NTRK1 | c.1517T= (p.Met506=) c.*289T= (n.*289T=) c.1697T= (p.Met566=) c.1688T= (p.Met563=) c.1679T= (p.Met560=) c.1589T= (p.Met530=) n.2150T= | |
| 1 | g.156876465G>A | CA342938521 | NTRK1 | c.1518G>A (p.Met506Ile) c.*290G>A (n.*290G>A) c.1698G>A (p.Met566Ile) c.1689G>A (p.Met563Ile) c.1680G>A (p.Met560Ile) c.1590G>A (p.Met530Ile) n.2151G>A | dbSNP |
| 1 | g.156876465G>C | CA342938522 | NTRK1 | c.1518G>C (p.Met506Ile) c.*290G>C (n.*290G>C) c.1698G>C (p.Met566Ile) c.1689G>C (p.Met563Ile) c.1680G>C (p.Met560Ile) c.1590G>C (p.Met530Ile) n.2151G>C | dbSNP |
| 1 | g.156876465G>T | CA342938523 | NTRK1 | c.1518G>T (p.Met506Ile) c.*290G>T (n.*290G>T) c.1698G>T (p.Met566Ile) c.1689G>T (p.Met563Ile) c.1680G>T (p.Met560Ile) c.1590G>T (p.Met530Ile) n.2151G>T | dbSNP |
| 1 | g.156876466C>A | CA342938524 | NTRK1 | c.1519C>A (p.Leu507Met) c.*291C>A (n.*291C>A) c.1699C>A (p.Leu567Met) c.1690C>A (p.Leu564Met) c.1681C>A (p.Leu561Met) c.1591C>A (p.Leu531Met) n.2152C>A | |
| 1 | g.156876466C>G | CA342938525 | NTRK1 | c.1519C>G (p.Leu507Val) c.*291C>G (n.*291C>G) c.1699C>G (p.Leu567Val) c.1690C>G (p.Leu564Val) c.1681C>G (p.Leu561Val) c.1591C>G (p.Leu531Val) n.2152C>G | dbSNP gnomAD v4 |
| 1 | g.156876466C>T | CA421138705 | NTRK1 | c.1519C>T (p.Leu507=) c.*291C>T (n.*291C>T) c.1699C>T (p.Leu567=) c.1690C>T (p.Leu564=) c.1681C>T (p.Leu561=) c.1591C>T (p.Leu531=) n.2152C>T | dbSNP COSMIC COSMIC |
| 1 | g.156876467T>A | CA342938528 | NTRK1 | c.1520T>A (p.Leu507Gln) c.*292T>A (n.*292T>A) c.1700T>A (p.Leu567Gln) c.1691T>A (p.Leu564Gln) c.1682T>A (p.Leu561Gln) c.1592T>A (p.Leu531Gln) n.2153T>A | dbSNP |
| 1 | g.156876467T>C | CA342938526 | NTRK1 | c.1520T>C (p.Leu507Pro) c.*292T>C (n.*292T>C) c.1700T>C (p.Leu567Pro) c.1691T>C (p.Leu564Pro) c.1682T>C (p.Leu561Pro) c.1592T>C (p.Leu531Pro) n.2153T>C | |
| 1 | g.156876467T>G | CA342938527 | NTRK1 | c.1520T>G (p.Leu507Arg) c.*292T>G (n.*292T>G) c.1700T>G (p.Leu567Arg) c.1691T>G (p.Leu564Arg) c.1682T>G (p.Leu561Arg) c.1592T>G (p.Leu531Arg) n.2153T>G | |
| 1 | g.156876468G>A | CA421138714 | NTRK1 | c.1521G>A (p.Leu507=) c.*293G>A (n.*293G>A) c.1701G>A (p.Leu567=) c.1692G>A (p.Leu564=) c.1683G>A (p.Leu561=) c.1593G>A (p.Leu531=) n.2154G>A | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876468G>C | CA421138716 | NTRK1 | c.1521G>C (p.Leu507=) c.*293G>C (n.*293G>C) c.1701G>C (p.Leu567=) c.1692G>C (p.Leu564=) c.1683G>C (p.Leu561=) c.1593G>C (p.Leu531=) n.2154G>C | |
| 1 | g.156876468G= | CA1200786107 | NTRK1 | c.1521G= (p.Leu507=) c.*293G= (n.*293G=) c.1701G= (p.Leu567=) c.1692G= (p.Leu564=) c.1683G= (p.Leu561=) c.1593G= (p.Leu531=) n.2154G= | |
| 1 | g.156876468G>T | CA421138718 | NTRK1 | c.1521G>T (p.Leu507=) c.*293G>T (n.*293G>T) c.1701G>T (p.Leu567=) c.1692G>T (p.Leu564=) c.1683G>T (p.Leu561=) c.1593G>T (p.Leu531=) n.2154G>T | |
| 1 | g.156876468_156876474delinsGCAGCAC | CA1200786106 | NTRK1 | c.1521_1527delinsGCAGCAC (p.Leu507=) c.*293_*299delinsGCAGCAC (n.*293_*299delinsGCAGCAC) c.1701_1707delinsGCAGCAC (p.Leu567=) c.1692_1698delinsGCAGCAC (p.Leu564=) c.1683_1689delinsGCAGCAC (p.Leu561=) c.1593_1599delinsGCAGCAC (p.Leu531=) n.2154_2160delinsGCAGCAC | |
| 1 | g.156876469C>A | CA342938529 | NTRK1 | c.1522C>A (p.Gln508Lys) c.*294C>A (n.*294C>A) c.1702C>A (p.Gln568Lys) c.1693C>A (p.Gln565Lys) c.1684C>A (p.Gln562Lys) c.1594C>A (p.Gln532Lys) n.2155C>A | dbSNP |
| 1 | g.156876469C>G | CA342938530 | NTRK1 | c.1522C>G (p.Gln508Glu) c.*294C>G (n.*294C>G) c.1702C>G (p.Gln568Glu) c.1693C>G (p.Gln565Glu) c.1684C>G (p.Gln562Glu) c.1594C>G (p.Gln532Glu) n.2155C>G | dbSNP |
| 1 | g.156876469C>T | CA342938531 | NTRK1 | c.1522C>T (p.Gln508Ter) c.*294C>T (n.*294C>T) c.1702C>T (p.Gln568Ter) c.1693C>T (p.Gln565Ter) c.1684C>T (p.Gln562Ter) c.1594C>T (p.Gln532Ter) n.2155C>T | dbSNP |
| 1 | g.156876475_156876480dup | CA1200786108 | NTRK1 | c.1528_1533dup (p.His511_Ile512insGlnHis) c.*300_*305dup (n.*300_*305dup) c.1708_1713dup (p.His571_Ile572insGlnHis) c.1699_1704dup (p.His568_Ile569insGlnHis) c.1690_1695dup (p.His565_Ile566insGlnHis) c.1600_1605dup (p.His535_Ile536insGlnHis) n.2161_2166dup | dbSNP |
| 1 | g.156876475_156876480del | CA889790125 | NTRK1 | c.1528_1533del (p.Gln510_His511del) c.*300_*305del (n.*300_*305del) c.1708_1713del (p.Gln570_His571del) c.1699_1704del (p.Gln567_His568del) c.1690_1695del (p.Gln564_His565del) c.1600_1605del (p.Gln534_His535del) n.2161_2166del | dbSNP |
| 1 | g.156876470A= | CA1200786109 | NTRK1 | c.1523A= (p.Gln508=) c.*295A= (n.*295A=) c.1703A= (p.Gln568=) c.1694A= (p.Gln565=) c.1685A= (p.Gln562=) c.1595A= (p.Gln532=) n.2156A= | |
| 1 | g.156876470A>C | CA342938532 | NTRK1 | c.1523A>C (p.Gln508Pro) c.*295A>C (n.*295A>C) c.1703A>C (p.Gln568Pro) c.1694A>C (p.Gln565Pro) c.1685A>C (p.Gln562Pro) c.1595A>C (p.Gln532Pro) n.2156A>C | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876470A>G | CA342938533 | NTRK1 | c.1523A>G (p.Gln508Arg) c.*295A>G (n.*295A>G) c.1703A>G (p.Gln568Arg) c.1694A>G (p.Gln565Arg) c.1685A>G (p.Gln562Arg) c.1595A>G (p.Gln532Arg) n.2156A>G | dbSNP |
| 1 | g.156876470A>T | CA342938534 | NTRK1 | c.1523A>T (p.Gln508Leu) c.*295A>T (n.*295A>T) c.1703A>T (p.Gln568Leu) c.1694A>T (p.Gln565Leu) c.1685A>T (p.Gln562Leu) c.1595A>T (p.Gln532Leu) n.2156A>T | dbSNP |
| 1 | g.156876471G>A | CA421138730 | NTRK1 | c.1524G>A (p.Gln508=) c.*296G>A (n.*296G>A) c.1704G>A (p.Gln568=) c.1695G>A (p.Gln565=) c.1686G>A (p.Gln562=) c.1596G>A (p.Gln532=) n.2157G>A | dbSNP |
| 1 | g.156876471G>C | CA342938535 | NTRK1 | c.1524G>C (p.Gln508His) c.*296G>C (n.*296G>C) c.1704G>C (p.Gln568His) c.1695G>C (p.Gln565His) c.1686G>C (p.Gln562His) c.1596G>C (p.Gln532His) n.2157G>C | dbSNP |
| 1 | g.156876471G= | CA1200786110 | NTRK1 | c.1524G= (p.Gln508=) c.*296G= (n.*296G=) c.1704G= (p.Gln568=) c.1695G= (p.Gln565=) c.1686G= (p.Gln562=) c.1596G= (p.Gln532=) n.2157G= | |
| 1 | g.156876471G>T | CA342938536 | NTRK1 | c.1524G>T (p.Gln508His) c.*296G>T (n.*296G>T) c.1704G>T (p.Gln568His) c.1695G>T (p.Gln565His) c.1686G>T (p.Gln562His) c.1596G>T (p.Gln532His) n.2157G>T | |
| 1 | g.156876472C>A | CA342938537 | NTRK1 | c.1525C>A (p.His509Asn) c.*297C>A (n.*297C>A) c.1705C>A (p.His569Asn) c.1696C>A (p.His566Asn) c.1687C>A (p.His563Asn) c.1597C>A (p.His533Asn) n.2158C>A | dbSNP |
| 1 | g.156876472C>G | CA342938538 | NTRK1 | c.1525C>G (p.His509Asp) c.*297C>G (n.*297C>G) c.1705C>G (p.His569Asp) c.1696C>G (p.His566Asp) c.1687C>G (p.His563Asp) c.1597C>G (p.His533Asp) n.2158C>G | dbSNP |
| 1 | g.156876472C>T | CA342938539 | NTRK1 | c.1525C>T (p.His509Tyr) c.*297C>T (n.*297C>T) c.1705C>T (p.His569Tyr) c.1696C>T (p.His566Tyr) c.1687C>T (p.His563Tyr) c.1597C>T (p.His533Tyr) n.2158C>T | dbSNP |
| 1 | g.156876473_156876474dup | CA1169441 | NTRK1 | c.1526_1527dup (p.Gln510ThrfsTer?) c.*298_*299dup (n.*298_*299dup) c.1706_1707dup (p.Gln570ThrfsTer?) c.1697_1698dup (p.Gln567ThrfsTer?) c.1688_1689dup (p.Gln564ThrfsTer?) c.1598_1599dup (p.Gln534ThrfsTer?) n.2159_2160dup | ClinVar dbSNP ExAC |
| 1 | g.156876473A= | CA1148422696 | NTRK1 | c.1526A= (p.His509=) c.*298A= (n.*298A=) c.1706A= (p.His569=) c.1697A= (p.His566=) c.1688A= (p.His563=) c.1598A= (p.His533=) n.2159A= | |
| 1 | g.156876473A>C | CA342938540 | NTRK1 | c.1526A>C (p.His509Pro) c.*298A>C (n.*298A>C) c.1706A>C (p.His569Pro) c.1697A>C (p.His566Pro) c.1688A>C (p.His563Pro) c.1598A>C (p.His533Pro) n.2159A>C | |
| 1 | g.156876473A>G | CA1169442 | NTRK1 | c.1526A>G (p.His509Arg) c.*298A>G (n.*298A>G) c.1706A>G (p.His569Arg) c.1697A>G (p.His566Arg) c.1688A>G (p.His563Arg) c.1598A>G (p.His533Arg) n.2159A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876473A>T | CA342938541 | NTRK1 | c.1526A>T (p.His509Leu) c.*298A>T (n.*298A>T) c.1706A>T (p.His569Leu) c.1697A>T (p.His566Leu) c.1688A>T (p.His563Leu) c.1598A>T (p.His533Leu) n.2159A>T | dbSNP |
| 1 | g.156876473_156876474insAA | CA2746258620 | NTRK1 | c.1526_1527insAA (p.His509GlnfsTer?) c.*298_*299insAA (n.*298_*299insAA) c.1706_1707insAA (p.His569GlnfsTer?) c.1697_1698insAA (p.His566GlnfsTer?) c.1688_1689insAA (p.His563GlnfsTer?) c.1598_1599insAA (p.His533GlnfsTer?) n.2159_2160insAA | |
| 1 | g.156876474C>A | CA342938542 | NTRK1 | c.1527C>A (p.His509Gln) c.*299C>A (n.*299C>A) c.1707C>A (p.His569Gln) c.1698C>A (p.His566Gln) c.1689C>A (p.His563Gln) c.1599C>A (p.His533Gln) n.2160C>A | dbSNP |
| 1 | g.156876474C= | CA1200786112 | NTRK1 | c.1527C= (p.His509=) c.*299C= (n.*299C=) c.1707C= (p.His569=) c.1698C= (p.His566=) c.1689C= (p.His563=) c.1599C= (p.His533=) n.2160C= | |
| 1 | g.156876474C>G | CA342938543 | NTRK1 | c.1527C>G (p.His509Gln) c.*299C>G (n.*299C>G) c.1707C>G (p.His569Gln) c.1698C>G (p.His566Gln) c.1689C>G (p.His563Gln) c.1599C>G (p.His533Gln) n.2160C>G | dbSNP |
| 1 | g.156876474C>T | CA421138748 | NTRK1 | c.1527C>T (p.His509=) c.*299C>T (n.*299C>T) c.1707C>T (p.His569=) c.1698C>T (p.His566=) c.1689C>T (p.His563=) c.1599C>T (p.His533=) n.2160C>T | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876474_156876503delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG | CA1200786111 | NTRK1 | c.1527_1556delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG (p.His509=) c.*299_*328delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG (n.*299_*328delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG) c.1707_1736delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG (p.His569=) c.1698_1727delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG (p.His566=) c.1689_1718delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG (p.His563=) c.1599_1628delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG (p.His533=) n.2160_2189delinsCCAGCACATCGTGCGCTTCTTCGGCGTCTG | |
| 1 | g.156876475C>A | CA342938544 | NTRK1 | c.1528C>A (p.Gln510Lys) c.*300C>A (n.*300C>A) c.1708C>A (p.Gln570Lys) c.1699C>A (p.Gln567Lys) c.1690C>A (p.Gln564Lys) c.1600C>A (p.Gln534Lys) n.2161C>A | dbSNP |
| 1 | g.156876475C>G | CA342938545 | NTRK1 | c.1528C>G (p.Gln510Glu) c.*300C>G (n.*300C>G) c.1708C>G (p.Gln570Glu) c.1699C>G (p.Gln567Glu) c.1690C>G (p.Gln564Glu) c.1600C>G (p.Gln534Glu) n.2161C>G | dbSNP |
| 1 | g.156876475C>T | CA342938546 | NTRK1 | c.1528C>T (p.Gln510Ter) c.*300C>T (n.*300C>T) c.1708C>T (p.Gln570Ter) c.1699C>T (p.Gln567Ter) c.1690C>T (p.Gln564Ter) c.1600C>T (p.Gln534Ter) n.2161C>T | dbSNP |
| 1 | g.156876475_156876505delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA | CA1148712143 | NTRK1 | c.1528_1558delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA (p.Gln510=) c.*300_*330delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA (n.*300_*330delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA) c.1708_1738delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA (p.Gln570=) c.1699_1729delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA (p.Gln567=) c.1690_1720delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA (p.Gln564=) c.1600_1630delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA (p.Gln534=) n.2161_2191delinsCAGCACATCGTGCGCTTCTTCGGCGTCTGCA | |
| 1 | g.156876477_156876505del | CA1169443 | NTRK1 | c.1530_1558del (p.Gln510HisfsTer11) c.*302_*330del (n.*302_*330del) c.1710_1738del (p.Gln570HisfsTer11) c.1701_1729del (p.Gln567HisfsTer11) c.1692_1720del (p.Gln564HisfsTer11) c.1602_1630del (p.Gln534HisfsTer11) n.2163_2191del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876476A>C | CA342938547 | NTRK1 | c.1529A>C (p.Gln510Pro) c.*301A>C (n.*301A>C) c.1709A>C (p.Gln570Pro) c.1700A>C (p.Gln567Pro) c.1691A>C (p.Gln564Pro) c.1601A>C (p.Gln534Pro) n.2162A>C | dbSNP |
| 1 | g.156876476A>G | CA342938548 | NTRK1 | c.1529A>G (p.Gln510Arg) c.*301A>G (n.*301A>G) c.1709A>G (p.Gln570Arg) c.1700A>G (p.Gln567Arg) c.1691A>G (p.Gln564Arg) c.1601A>G (p.Gln534Arg) n.2162A>G | dbSNP |
| 1 | g.156876476A>T | CA342938549 | NTRK1 | c.1529A>T (p.Gln510Leu) c.*301A>T (n.*301A>T) c.1709A>T (p.Gln570Leu) c.1700A>T (p.Gln567Leu) c.1691A>T (p.Gln564Leu) c.1601A>T (p.Gln534Leu) n.2162A>T | dbSNP |
| 1 | g.156876477G>A | CA421138761 | NTRK1 | c.1530G>A (p.Gln510=) c.*302G>A (n.*302G>A) c.1710G>A (p.Gln570=) c.1701G>A (p.Gln567=) c.1692G>A (p.Gln564=) c.1602G>A (p.Gln534=) n.2163G>A | |
| 1 | g.156876477G>C | CA342938550 | NTRK1 | c.1530G>C (p.Gln510His) c.*302G>C (n.*302G>C) c.1710G>C (p.Gln570His) c.1701G>C (p.Gln567His) c.1692G>C (p.Gln564His) c.1602G>C (p.Gln534His) n.2163G>C | |
| 1 | g.156876477G>T | CA342938551 | NTRK1 | c.1530G>T (p.Gln510His) c.*302G>T (n.*302G>T) c.1710G>T (p.Gln570His) c.1701G>T (p.Gln567His) c.1692G>T (p.Gln564His) c.1602G>T (p.Gln534His) n.2163G>T | |
| 1 | g.156876478C>A | CA342938554 | NTRK1 | c.1531C>A (p.His511Asn) c.*303C>A (n.*303C>A) c.1711C>A (p.His571Asn) c.1702C>A (p.His568Asn) c.1693C>A (p.His565Asn) c.1603C>A (p.His535Asn) n.2164C>A | |
| 1 | g.156876478C>G | CA342938553 | NTRK1 | c.1531C>G (p.His511Asp) c.*303C>G (n.*303C>G) c.1711C>G (p.His571Asp) c.1702C>G (p.His568Asp) c.1693C>G (p.His565Asp) c.1603C>G (p.His535Asp) n.2164C>G | dbSNP |
| 1 | g.156876478C>T | CA342938552 | NTRK1 | c.1531C>T (p.His511Tyr) c.*303C>T (n.*303C>T) c.1711C>T (p.His571Tyr) c.1702C>T (p.His568Tyr) c.1693C>T (p.His565Tyr) c.1603C>T (p.His535Tyr) n.2164C>T | dbSNP |
| 1 | g.156876479A>C | CA342938555 | NTRK1 | c.1532A>C (p.His511Pro) c.*304A>C (n.*304A>C) c.1712A>C (p.His571Pro) c.1703A>C (p.His568Pro) c.1694A>C (p.His565Pro) c.1604A>C (p.His535Pro) n.2165A>C | dbSNP |
| 1 | g.156876479A>G | CA342938556 | NTRK1 | c.1532A>G (p.His511Arg) c.*304A>G (n.*304A>G) c.1712A>G (p.His571Arg) c.1703A>G (p.His568Arg) c.1694A>G (p.His565Arg) c.1604A>G (p.His535Arg) n.2165A>G | gnomAD v4 |
| 1 | g.156876479A>T | CA342938557 | NTRK1 | c.1532A>T (p.His511Leu) c.*304A>T (n.*304A>T) c.1712A>T (p.His571Leu) c.1703A>T (p.His568Leu) c.1694A>T (p.His565Leu) c.1604A>T (p.His535Leu) n.2165A>T | dbSNP |
| 1 | g.156876480C>A | CA342938558 | NTRK1 | c.1533C>A (p.His511Gln) c.*305C>A (n.*305C>A) c.1713C>A (p.His571Gln) c.1704C>A (p.His568Gln) c.1695C>A (p.His565Gln) c.1605C>A (p.His535Gln) n.2166C>A | ClinVar dbSNP |
| 1 | g.156876480C>G | CA342938559 | NTRK1 | c.1533C>G (p.His511Gln) c.*305C>G (n.*305C>G) c.1713C>G (p.His571Gln) c.1704C>G (p.His568Gln) c.1695C>G (p.His565Gln) c.1605C>G (p.His535Gln) n.2166C>G | dbSNP |
| 1 | g.156876480C>T | CA421138777 | NTRK1 | c.1533C>T (p.His511=) c.*305C>T (n.*305C>T) c.1713C>T (p.His571=) c.1704C>T (p.His568=) c.1695C>T (p.His565=) c.1605C>T (p.His535=) n.2166C>T | dbSNP gnomAD v4 |
| 1 | g.156876481A= | CA1200786113 | NTRK1 | c.1534A= (p.Ile512=) c.*306A= (n.*306A=) c.1714A= (p.Ile572=) c.1705A= (p.Ile569=) c.1696A= (p.Ile566=) c.1606A= (p.Ile536=) n.2167A= | |
| 1 | g.156876481A>C | CA342938560 | NTRK1 | c.1534A>C (p.Ile512Leu) c.*306A>C (n.*306A>C) c.1714A>C (p.Ile572Leu) c.1705A>C (p.Ile569Leu) c.1696A>C (p.Ile566Leu) c.1606A>C (p.Ile536Leu) n.2167A>C | dbSNP |
| 1 | g.156876481A>G | CA31118794 | NTRK1 | c.1534A>G (p.Ile512Val) c.*306A>G (n.*306A>G) c.1714A>G (p.Ile572Val) c.1705A>G (p.Ile569Val) c.1696A>G (p.Ile566Val) c.1606A>G (p.Ile536Val) n.2167A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876481A>T | CA342938561 | NTRK1 | c.1534A>T (p.Ile512Phe) c.*306A>T (n.*306A>T) c.1714A>T (p.Ile572Phe) c.1705A>T (p.Ile569Phe) c.1696A>T (p.Ile566Phe) c.1606A>T (p.Ile536Phe) n.2167A>T | dbSNP |
| 1 | g.156876482T>A | CA342938562 | NTRK1 | c.1535T>A (p.Ile512Asn) c.*307T>A (n.*307T>A) c.1715T>A (p.Ile572Asn) c.1706T>A (p.Ile569Asn) c.1697T>A (p.Ile566Asn) c.1607T>A (p.Ile536Asn) n.2168T>A | dbSNP |
| 1 | g.156876482T>C | CA342938563 | NTRK1 | c.1535T>C (p.Ile512Thr) c.*307T>C (n.*307T>C) c.1715T>C (p.Ile572Thr) c.1706T>C (p.Ile569Thr) c.1697T>C (p.Ile566Thr) c.1607T>C (p.Ile536Thr) n.2168T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876482T>G | CA342938564 | NTRK1 | c.1535T>G (p.Ile512Ser) c.*307T>G (n.*307T>G) c.1715T>G (p.Ile572Ser) c.1706T>G (p.Ile569Ser) c.1697T>G (p.Ile566Ser) c.1607T>G (p.Ile536Ser) n.2168T>G | |
| 1 | g.156876482T= | CA1200786114 | NTRK1 | c.1535T= (p.Ile512=) c.*307T= (n.*307T=) c.1715T= (p.Ile572=) c.1706T= (p.Ile569=) c.1697T= (p.Ile566=) c.1607T= (p.Ile536=) n.2168T= | |
| 1 | g.156876483C>A | CA421138785 | NTRK1 | c.1536C>A (p.Ile512=) c.*308C>A (n.*308C>A) c.1716C>A (p.Ile572=) c.1707C>A (p.Ile569=) c.1698C>A (p.Ile566=) c.1608C>A (p.Ile536=) n.2169C>A | dbSNP gnomAD v4 |
| 1 | g.156876483C= | CA1200786115 | NTRK1 | c.1536C= (p.Ile512=) c.*308C= (n.*308C=) c.1716C= (p.Ile572=) c.1707C= (p.Ile569=) c.1698C= (p.Ile566=) c.1608C= (p.Ile536=) n.2169C= | |
| 1 | g.156876483C>G | CA342938565 | NTRK1 | c.1536C>G (p.Ile512Met) c.*308C>G (n.*308C>G) c.1716C>G (p.Ile572Met) c.1707C>G (p.Ile569Met) c.1698C>G (p.Ile566Met) c.1608C>G (p.Ile536Met) n.2169C>G | dbSNP |
| 1 | g.156876483C>T | CA31118810 | NTRK1 | c.1536C>T (p.Ile512=) c.*308C>T (n.*308C>T) c.1716C>T (p.Ile572=) c.1707C>T (p.Ile569=) c.1698C>T (p.Ile566=) c.1608C>T (p.Ile536=) n.2169C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.156876484G>A | CA1169444 | NTRK1 | c.1537G>A (p.Val513Met) c.*309G>A (n.*309G>A) c.1717G>A (p.Val573Met) c.1708G>A (p.Val570Met) c.1699G>A (p.Val567Met) c.1609G>A (p.Val537Met) n.2170G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876484G>C | CA342938567 | NTRK1 | c.1537G>C (p.Val513Leu) c.*309G>C (n.*309G>C) c.1717G>C (p.Val573Leu) c.1708G>C (p.Val570Leu) c.1699G>C (p.Val567Leu) c.1609G>C (p.Val537Leu) n.2170G>C | dbSNP |
| 1 | g.156876484G= | CA1200786116 | NTRK1 | c.1537G= (p.Val513=) c.*309G= (n.*309G=) c.1717G= (p.Val573=) c.1708G= (p.Val570=) c.1699G= (p.Val567=) c.1609G= (p.Val537=) n.2170G= | |
| 1 | g.156876484G>T | CA342938566 | NTRK1 | c.1537G>T (p.Val513Leu) c.*309G>T (n.*309G>T) c.1717G>T (p.Val573Leu) c.1708G>T (p.Val570Leu) c.1699G>T (p.Val567Leu) c.1609G>T (p.Val537Leu) n.2170G>T | dbSNP gnomAD v4 |
| 1 | g.156876485T>A | CA342938568 | NTRK1 | c.1538T>A (p.Val513Glu) c.*310T>A (n.*310T>A) c.1718T>A (p.Val573Glu) c.1709T>A (p.Val570Glu) c.1700T>A (p.Val567Glu) c.1610T>A (p.Val537Glu) n.2171T>A | dbSNP |
| 1 | g.156876485T>C | CA342938569 | NTRK1 | c.1538T>C (p.Val513Ala) c.*310T>C (n.*310T>C) c.1718T>C (p.Val573Ala) c.1709T>C (p.Val570Ala) c.1700T>C (p.Val567Ala) c.1610T>C (p.Val537Ala) n.2171T>C | dbSNP gnomAD v4 |
| 1 | g.156876485T>G | CA342938570 | NTRK1 | c.1538T>G (p.Val513Gly) c.*310T>G (n.*310T>G) c.1718T>G (p.Val573Gly) c.1709T>G (p.Val570Gly) c.1700T>G (p.Val567Gly) c.1610T>G (p.Val537Gly) n.2171T>G | dbSNP |
| 1 | g.156876485T= | CA1200786117 | NTRK1 | c.1538T= (p.Val513=) c.*310T= (n.*310T=) c.1718T= (p.Val573=) c.1709T= (p.Val570=) c.1700T= (p.Val567=) c.1610T= (p.Val537=) n.2171T= | |
| 1 | g.156876486G>A | CA1169445 | NTRK1 | c.1539G>A (p.Val513=) c.*311G>A (n.*311G>A) c.1719G>A (p.Val573=) c.1710G>A (p.Val570=) c.1701G>A (p.Val567=) c.1611G>A (p.Val537=) n.2172G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876486G>C | CA421138802 | NTRK1 | c.1539G>C (p.Val513=) c.*311G>C (n.*311G>C) c.1719G>C (p.Val573=) c.1710G>C (p.Val570=) c.1701G>C (p.Val567=) c.1611G>C (p.Val537=) n.2172G>C | dbSNP |
| 1 | g.156876486G= | CA1200786118 | NTRK1 | c.1539G= (p.Val513=) c.*311G= (n.*311G=) c.1719G= (p.Val573=) c.1710G= (p.Val570=) c.1701G= (p.Val567=) c.1611G= (p.Val537=) n.2172G= | |
| 1 | g.156876486G>T | CA421138804 | NTRK1 | c.1539G>T (p.Val513=) c.*311G>T (n.*311G>T) c.1719G>T (p.Val573=) c.1710G>T (p.Val570=) c.1701G>T (p.Val567=) c.1611G>T (p.Val537=) n.2172G>T | COSMIC COSMIC |
| 1 | g.156876487C>A | CA342938571 | NTRK1 | c.1540C>A (p.Arg514Ser) c.*312C>A (n.*312C>A) c.1720C>A (p.Arg574Ser) c.1711C>A (p.Arg571Ser) c.1702C>A (p.Arg568Ser) c.1612C>A (p.Arg538Ser) n.2173C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876487C= | CA1143622333 | NTRK1 | c.1540C= (p.Arg514=) c.*312C= (n.*312C=) c.1720C= (p.Arg574=) c.1711C= (p.Arg571=) c.1702C= (p.Arg568=) c.1612C= (p.Arg538=) n.2173C= | |
| 1 | g.156876487C>G | CA342938572 | NTRK1 | c.1540C>G (p.Arg514Gly) c.*312C>G (n.*312C>G) c.1720C>G (p.Arg574Gly) c.1711C>G (p.Arg571Gly) c.1702C>G (p.Arg568Gly) c.1612C>G (p.Arg538Gly) n.2173C>G | dbSNP |
| 1 | g.156876487C>T | CA31118816 | NTRK1 | c.1540C>T (p.Arg514Cys) c.*312C>T (n.*312C>T) c.1720C>T (p.Arg574Cys) c.1711C>T (p.Arg571Cys) c.1702C>T (p.Arg568Cys) c.1612C>T (p.Arg538Cys) n.2173C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876489_156876496dup | CA2648464199 | NTRK1 | c.1542_1549dup (p.Gly517AlafsTer?) c.*314_*321dup (n.*314_*321dup) c.1722_1729dup (p.Gly577AlafsTer?) c.1713_1720dup (p.Gly574AlafsTer?) c.1704_1711dup (p.Gly571AlafsTer?) c.1614_1621dup (p.Gly541AlafsTer?) n.2175_2182dup | gnomAD v4 |
| 1 | g.156876488G>A | CA1169446 | NTRK1 | c.1541G>A (p.Arg514His) c.*313G>A (n.*313G>A) c.1721G>A (p.Arg574His) c.1712G>A (p.Arg571His) c.1703G>A (p.Arg568His) c.1613G>A (p.Arg538His) n.2174G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876488G>C | CA342938574 | NTRK1 | c.1541G>C (p.Arg514Pro) c.*313G>C (n.*313G>C) c.1721G>C (p.Arg574Pro) c.1712G>C (p.Arg571Pro) c.1703G>C (p.Arg568Pro) c.1613G>C (p.Arg538Pro) n.2174G>C | |
| 1 | g.156876488G= | CA1146287321 | NTRK1 | c.1541G= (p.Arg514=) c.*313G= (n.*313G=) c.1721G= (p.Arg574=) c.1712G= (p.Arg571=) c.1703G= (p.Arg568=) c.1613G= (p.Arg538=) n.2174G= | |
| 1 | g.156876488G>T | CA342938573 | NTRK1 | c.1541G>T (p.Arg514Leu) c.*313G>T (n.*313G>T) c.1721G>T (p.Arg574Leu) c.1712G>T (p.Arg571Leu) c.1703G>T (p.Arg568Leu) c.1613G>T (p.Arg538Leu) n.2174G>T | |
| 1 | g.156876489C>A | CA421138814 | NTRK1 | c.1542C>A (p.Arg514=) c.*314C>A (n.*314C>A) c.1722C>A (p.Arg574=) c.1713C>A (p.Arg571=) c.1704C>A (p.Arg568=) c.1614C>A (p.Arg538=) n.2175C>A | |
| 1 | g.156876489C= | CA1143686397 | NTRK1 | c.1542C= (p.Arg514=) c.*314C= (n.*314C=) c.1722C= (p.Arg574=) c.1713C= (p.Arg571=) c.1704C= (p.Arg568=) c.1614C= (p.Arg538=) n.2175C= | |
| 1 | g.156876489C>G | CA421138816 | NTRK1 | c.1542C>G (p.Arg514=) c.*314C>G (n.*314C>G) c.1722C>G (p.Arg574=) c.1713C>G (p.Arg571=) c.1704C>G (p.Arg568=) c.1614C>G (p.Arg538=) n.2175C>G | dbSNP |
| 1 | g.156876489C>T | CA31118847 | NTRK1 | c.1542C>T (p.Arg514=) c.*314C>T (n.*314C>T) c.1722C>T (p.Arg574=) c.1713C>T (p.Arg571=) c.1704C>T (p.Arg568=) c.1614C>T (p.Arg538=) n.2175C>T | ClinVar dbSNP |
| 1 | g.156876493_156876495dup | CA1200786119 | NTRK1 | c.1546_1548dup (p.Phe516_Gly517insPhe) c.*318_*320dup (n.*318_*320dup) c.1726_1728dup (p.Phe576_Gly577insPhe) c.1717_1719dup (p.Phe573_Gly574insPhe) c.1708_1710dup (p.Phe570_Gly571insPhe) c.1618_1620dup (p.Phe540_Gly541insPhe) n.2179_2181dup | dbSNP |
| 1 | g.156876490T>A | CA342938575 | NTRK1 | c.1543T>A (p.Phe515Ile) c.*315T>A (n.*315T>A) c.1723T>A (p.Phe575Ile) c.1714T>A (p.Phe572Ile) c.1705T>A (p.Phe569Ile) c.1615T>A (p.Phe539Ile) n.2176T>A | |
| 1 | g.156876490T>C | CA1169447 | NTRK1 | c.1543T>C (p.Phe515Leu) c.*315T>C (n.*315T>C) c.1723T>C (p.Phe575Leu) c.1714T>C (p.Phe572Leu) c.1705T>C (p.Phe569Leu) c.1615T>C (p.Phe539Leu) n.2176T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876490T>G | CA342938576 | NTRK1 | c.1543T>G (p.Phe515Val) c.*315T>G (n.*315T>G) c.1723T>G (p.Phe575Val) c.1714T>G (p.Phe572Val) c.1705T>G (p.Phe569Val) c.1615T>G (p.Phe539Val) n.2176T>G | |
| 1 | g.156876490T= | CA1200786120 | NTRK1 | c.1543T= (p.Phe515=) c.*315T= (n.*315T=) c.1723T= (p.Phe575=) c.1714T= (p.Phe572=) c.1705T= (p.Phe569=) c.1615T= (p.Phe539=) n.2176T= | |
| 1 | g.156876491del | CA2746258621 | NTRK1 | c.1544del (p.Phe515SerfsTer?) c.*316del (n.*316del) c.1724del (p.Phe575SerfsTer?) c.1715del (p.Phe572SerfsTer?) c.1706del (p.Phe569SerfsTer?) c.1616del (p.Phe539SerfsTer?) n.2177del | |
| 1 | g.156876490_156876499delinsTTCTTCGGCG | CA1200786121 | NTRK1 | c.1543_1552delinsTTCTTCGGCG (p.Phe515=) c.*315_*324delinsTTCTTCGGCG (n.*315_*324delinsTTCTTCGGCG) c.1723_1732delinsTTCTTCGGCG (p.Phe575=) c.1714_1723delinsTTCTTCGGCG (p.Phe572=) c.1705_1714delinsTTCTTCGGCG (p.Phe569=) c.1615_1624delinsTTCTTCGGCG (p.Phe539=) n.2176_2185delinsTTCTTCGGCG | |
| 1 | g.156876491T>A | CA342938579 | NTRK1 | c.1544T>A (p.Phe515Tyr) c.*316T>A (n.*316T>A) c.1724T>A (p.Phe575Tyr) c.1715T>A (p.Phe572Tyr) c.1706T>A (p.Phe569Tyr) c.1616T>A (p.Phe539Tyr) n.2177T>A | |
| 1 | g.156876491T>C | CA342938577 | NTRK1 | c.1544T>C (p.Phe515Ser) c.*316T>C (n.*316T>C) c.1724T>C (p.Phe575Ser) c.1715T>C (p.Phe572Ser) c.1706T>C (p.Phe569Ser) c.1616T>C (p.Phe539Ser) n.2177T>C | dbSNP |
| 1 | g.156876491T>G | CA342938578 | NTRK1 | c.1544T>G (p.Phe515Cys) c.*316T>G (n.*316T>G) c.1724T>G (p.Phe575Cys) c.1715T>G (p.Phe572Cys) c.1706T>G (p.Phe569Cys) c.1616T>G (p.Phe539Cys) n.2177T>G | |
| 1 | g.156876494_156876502del | CA1200786122 | NTRK1 | c.1547_1555del (p.Phe516_Val518del) c.*319_*327del (n.*319_*327del) c.1727_1735del (p.Phe576_Val578del) c.1718_1726del (p.Phe573_Val575del) c.1709_1717del (p.Phe570_Val572del) c.1619_1627del (p.Phe540_Val542del) n.2180_2188del | ClinVar dbSNP |
| 1 | g.156876492C>A | CA342938580 | NTRK1 | c.1545C>A (p.Phe515Leu) c.*317C>A (n.*317C>A) c.1725C>A (p.Phe575Leu) c.1716C>A (p.Phe572Leu) c.1707C>A (p.Phe569Leu) c.1617C>A (p.Phe539Leu) n.2178C>A | dbSNP |
| 1 | g.156876492C>G | CA342938581 | NTRK1 | c.1545C>G (p.Phe515Leu) c.*317C>G (n.*317C>G) c.1725C>G (p.Phe575Leu) c.1716C>G (p.Phe572Leu) c.1707C>G (p.Phe569Leu) c.1617C>G (p.Phe539Leu) n.2178C>G | dbSNP |
| 1 | g.156876492C>T | CA421138830 | NTRK1 | c.1545C>T (p.Phe515=) c.*317C>T (n.*317C>T) c.1725C>T (p.Phe575=) c.1716C>T (p.Phe572=) c.1707C>T (p.Phe569=) c.1617C>T (p.Phe539=) n.2178C>T | dbSNP gnomAD v4 |
| 1 | g.156876493T>A | CA342938582 | NTRK1 | c.1546T>A (p.Phe516Ile) c.*318T>A (n.*318T>A) c.1726T>A (p.Phe576Ile) c.1717T>A (p.Phe573Ile) c.1708T>A (p.Phe570Ile) c.1618T>A (p.Phe540Ile) n.2179T>A | |
| 1 | g.156876493T>C | CA342938583 | NTRK1 | c.1546T>C (p.Phe516Leu) c.*318T>C (n.*318T>C) c.1726T>C (p.Phe576Leu) c.1717T>C (p.Phe573Leu) c.1708T>C (p.Phe570Leu) c.1618T>C (p.Phe540Leu) n.2179T>C | |
| 1 | g.156876493T>G | CA342938584 | NTRK1 | c.1546T>G (p.Phe516Val) c.*318T>G (n.*318T>G) c.1726T>G (p.Phe576Val) c.1717T>G (p.Phe573Val) c.1708T>G (p.Phe570Val) c.1618T>G (p.Phe540Val) n.2179T>G | |
| 1 | g.156876494T>A | CA342938587 | NTRK1 | c.1547T>A (p.Phe516Tyr) c.*319T>A (n.*319T>A) c.1727T>A (p.Phe576Tyr) c.1718T>A (p.Phe573Tyr) c.1709T>A (p.Phe570Tyr) c.1619T>A (p.Phe540Tyr) n.2180T>A | dbSNP |
| 1 | g.156876494T>C | CA342938586 | NTRK1 | c.1547T>C (p.Phe516Ser) c.*319T>C (n.*319T>C) c.1727T>C (p.Phe576Ser) c.1718T>C (p.Phe573Ser) c.1709T>C (p.Phe570Ser) c.1619T>C (p.Phe540Ser) n.2180T>C | dbSNP |
| 1 | g.156876494T>G | CA342938585 | NTRK1 | c.1547T>G (p.Phe516Cys) c.*319T>G (n.*319T>G) c.1727T>G (p.Phe576Cys) c.1718T>G (p.Phe573Cys) c.1709T>G (p.Phe570Cys) c.1619T>G (p.Phe540Cys) n.2180T>G | |
| 1 | g.156876495C>A | CA342938588 | NTRK1 | c.1548C>A (p.Phe516Leu) c.*320C>A (n.*320C>A) c.1728C>A (p.Phe576Leu) c.1719C>A (p.Phe573Leu) c.1710C>A (p.Phe570Leu) c.1620C>A (p.Phe540Leu) n.2181C>A | dbSNP gnomAD v4 |
| 1 | g.156876495C= | CA1139773136 | NTRK1 | c.1548C= (p.Phe516=) c.*320C= (n.*320C=) c.1728C= (p.Phe576=) c.1719C= (p.Phe573=) c.1710C= (p.Phe570=) c.1620C= (p.Phe540=) n.2181C= | |
| 1 | g.156876495C>G | CA342938589 | NTRK1 | c.1548C>G (p.Phe516Leu) c.*320C>G (n.*320C>G) c.1728C>G (p.Phe576Leu) c.1719C>G (p.Phe573Leu) c.1710C>G (p.Phe570Leu) c.1620C>G (p.Phe540Leu) n.2181C>G | dbSNP |
| 1 | g.156876495C>T | CA1169448 | NTRK1 | c.1548C>T (p.Phe516=) c.*320C>T (n.*320C>T) c.1728C>T (p.Phe576=) c.1719C>T (p.Phe573=) c.1710C>T (p.Phe570=) c.1620C>T (p.Phe540=) n.2181C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876497_156876499dup | CA2648464230 | NTRK1 | c.1550_1552dup (p.Gly517_Val518insGly) c.*322_*324dup (n.*322_*324dup) c.1730_1732dup (p.Gly577_Val578insGly) c.1721_1723dup (p.Gly574_Val575insGly) c.1712_1714dup (p.Gly571_Val572insGly) c.1622_1624dup (p.Gly541_Val542insGly) n.2183_2185dup | gnomAD v4 |
| 1 | g.156876496_156876506del | CA2586964229 | NTRK1 | c.1549_1559del (p.Gly517ArgfsTer10) c.*321_*331del (n.*321_*331del) c.1729_1739del (p.Gly577ArgfsTer10) c.1720_1730del (p.Gly574ArgfsTer10) c.1711_1721del (p.Gly571ArgfsTer10) c.1621_1631del (p.Gly541ArgfsTer10) n.2182_2192del | |
| 1 | g.156876496G>A | CA1169449 | NTRK1 | c.1549G>A (p.Gly517Ser) c.*321G>A (n.*321G>A) c.1729G>A (p.Gly577Ser) c.1720G>A (p.Gly574Ser) c.1711G>A (p.Gly571Ser) c.1621G>A (p.Gly541Ser) n.2182G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876496G>C | CA256262 | NTRK1 | c.1549G>C (p.Gly517Arg) c.*321G>C (n.*321G>C) c.1729G>C (p.Gly577Arg) c.1720G>C (p.Gly574Arg) c.1711G>C (p.Gly571Arg) c.1621G>C (p.Gly541Arg) n.2182G>C | ClinVar dbSNP |
| 1 | g.156876496G= | CA1141581093 | NTRK1 | c.1549G= (p.Gly517=) c.*321G= (n.*321G=) c.1729G= (p.Gly577=) c.1720G= (p.Gly574=) c.1711G= (p.Gly571=) c.1621G= (p.Gly541=) n.2182G= | |
| 1 | g.156876496G>T | CA342938590 | NTRK1 | c.1549G>T (p.Gly517Cys) c.*321G>T (n.*321G>T) c.1729G>T (p.Gly577Cys) c.1720G>T (p.Gly574Cys) c.1711G>T (p.Gly571Cys) c.1621G>T (p.Gly541Cys) n.2182G>T | dbSNP |
| 1 | g.156876497del | CA2648464243 | NTRK1 | c.1550del (p.Gly517AlafsTer?) c.*322del (n.*322del) c.1730del (p.Gly577AlafsTer?) c.1721del (p.Gly574AlafsTer?) c.1712del (p.Gly571AlafsTer?) c.1622del (p.Gly541AlafsTer?) n.2183del | gnomAD v4 |
| 1 | g.156876497_156876503dup | CA2580061231 | NTRK1 | c.1550_1556dup (p.Cys519TrpfsTer14) c.*322_*328dup (n.*322_*328dup) c.1730_1736dup (p.Cys579TrpfsTer14) c.1721_1727dup (p.Cys576TrpfsTer14) c.1712_1718dup (p.Cys573TrpfsTer14) c.1622_1628dup (p.Cys543TrpfsTer14) n.2183_2189dup | ClinVar |
| 1 | g.156876497G>A | CA1169450 | NTRK1 | c.1550G>A (p.Gly517Asp) c.*322G>A (n.*322G>A) c.1730G>A (p.Gly577Asp) c.1721G>A (p.Gly574Asp) c.1712G>A (p.Gly571Asp) c.1622G>A (p.Gly541Asp) n.2183G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876497G>C | CA342938592 | NTRK1 | c.1550G>C (p.Gly517Ala) c.*322G>C (n.*322G>C) c.1730G>C (p.Gly577Ala) c.1721G>C (p.Gly574Ala) c.1712G>C (p.Gly571Ala) c.1622G>C (p.Gly541Ala) n.2183G>C | dbSNP |
| 1 | g.156876497G= | CA1200786123 | NTRK1 | c.1550G= (p.Gly517=) c.*322G= (n.*322G=) c.1730G= (p.Gly577=) c.1721G= (p.Gly574=) c.1712G= (p.Gly571=) c.1622G= (p.Gly541=) n.2183G= | |
| 1 | g.156876497G>T | CA342938591 | NTRK1 | c.1550G>T (p.Gly517Val) c.*322G>T (n.*322G>T) c.1730G>T (p.Gly577Val) c.1721G>T (p.Gly574Val) c.1712G>T (p.Gly571Val) c.1622G>T (p.Gly541Val) n.2183G>T | dbSNP |
| 1 | g.156876498C>A | CA421138856 | NTRK1 | c.1551C>A (p.Gly517=) c.*323C>A (n.*323C>A) c.1731C>A (p.Gly577=) c.1722C>A (p.Gly574=) c.1713C>A (p.Gly571=) c.1623C>A (p.Gly541=) n.2184C>A | dbSNP |
| 1 | g.156876498C= | CA1200786124 | NTRK1 | c.1551C= (p.Gly517=) c.*323C= (n.*323C=) c.1731C= (p.Gly577=) c.1722C= (p.Gly574=) c.1713C= (p.Gly571=) c.1623C= (p.Gly541=) n.2184C= | |
| 1 | g.156876498C>G | CA421138858 | NTRK1 | c.1551C>G (p.Gly517=) c.*323C>G (n.*323C>G) c.1731C>G (p.Gly577=) c.1722C>G (p.Gly574=) c.1713C>G (p.Gly571=) c.1623C>G (p.Gly541=) n.2184C>G | dbSNP |
| 1 | g.156876498C>T | CA1169451 | NTRK1 | c.1551C>T (p.Gly517=) c.*323C>T (n.*323C>T) c.1731C>T (p.Gly577=) c.1722C>T (p.Gly574=) c.1713C>T (p.Gly571=) c.1623C>T (p.Gly541=) n.2184C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.156876499G>A | CA1169452 | NTRK1 | c.1552G>A (p.Val518Ile) c.*324G>A (n.*324G>A) c.1732G>A (p.Val578Ile) c.1723G>A (p.Val575Ile) c.1714G>A (p.Val572Ile) c.1624G>A (p.Val542Ile) n.2185G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876499G>C | CA342938593 | NTRK1 | c.1552G>C (p.Val518Leu) c.*324G>C (n.*324G>C) c.1732G>C (p.Val578Leu) c.1723G>C (p.Val575Leu) c.1714G>C (p.Val572Leu) c.1624G>C (p.Val542Leu) n.2185G>C | dbSNP |
| 1 | g.156876499G= | CA1200786125 | NTRK1 | c.1552G= (p.Val518=) c.*324G= (n.*324G=) c.1732G= (p.Val578=) c.1723G= (p.Val575=) c.1714G= (p.Val572=) c.1624G= (p.Val542=) n.2185G= | |
| 1 | g.156876499G>T | CA342938594 | NTRK1 | c.1552G>T (p.Val518Phe) c.*324G>T (n.*324G>T) c.1732G>T (p.Val578Phe) c.1723G>T (p.Val575Phe) c.1714G>T (p.Val572Phe) c.1624G>T (p.Val542Phe) n.2185G>T | |
| 1 | g.156876500T>A | CA342938595 | NTRK1 | c.1553T>A (p.Val518Asp) c.*325T>A (n.*325T>A) c.1733T>A (p.Val578Asp) c.1724T>A (p.Val575Asp) c.1715T>A (p.Val572Asp) c.1625T>A (p.Val542Asp) n.2186T>A | dbSNP |
| 1 | g.156876500T>C | CA342938596 | NTRK1 | c.1553T>C (p.Val518Ala) c.*325T>C (n.*325T>C) c.1733T>C (p.Val578Ala) c.1724T>C (p.Val575Ala) c.1715T>C (p.Val572Ala) c.1625T>C (p.Val542Ala) n.2186T>C | dbSNP |
| 1 | g.156876500T>G | CA342938597 | NTRK1 | c.1553T>G (p.Val518Gly) c.*325T>G (n.*325T>G) c.1733T>G (p.Val578Gly) c.1724T>G (p.Val575Gly) c.1715T>G (p.Val572Gly) c.1625T>G (p.Val542Gly) n.2186T>G | ClinVar dbSNP |
| 1 | g.156876500T= | CA1200786126 | NTRK1 | c.1553T= (p.Val518=) c.*325T= (n.*325T=) c.1733T= (p.Val578=) c.1724T= (p.Val575=) c.1715T= (p.Val572=) c.1625T= (p.Val542=) n.2186T= | |
| 1 | g.156876501C>A | CA421138866 | NTRK1 | c.1554C>A (p.Val518=) c.*326C>A (n.*326C>A) c.1734C>A (p.Val578=) c.1725C>A (p.Val575=) c.1716C>A (p.Val572=) c.1626C>A (p.Val542=) n.2187C>A | dbSNP |
| 1 | g.156876501C= | CA1200786127 | NTRK1 | c.1554C= (p.Val518=) c.*326C= (n.*326C=) c.1734C= (p.Val578=) c.1725C= (p.Val575=) c.1716C= (p.Val572=) c.1626C= (p.Val542=) n.2187C= | |
| 1 | g.156876501C>G | CA31118886 | NTRK1 | c.1554C>G (p.Val518=) c.*326C>G (n.*326C>G) c.1734C>G (p.Val578=) c.1725C>G (p.Val575=) c.1716C>G (p.Val572=) c.1626C>G (p.Val542=) n.2187C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876501C>T | CA421138868 | NTRK1 | c.1554C>T (p.Val518=) c.*326C>T (n.*326C>T) c.1734C>T (p.Val578=) c.1725C>T (p.Val575=) c.1716C>T (p.Val572=) c.1626C>T (p.Val542=) n.2187C>T | dbSNP |
| 1 | g.156876505_156876523dup | CA2648464276 | NTRK1 | c.1558_1576dup (p.Leu526HisfsTer11) c.*330_*348dup (n.*330_*348dup) c.1738_1756dup (p.Leu586HisfsTer11) c.1729_1747dup (p.Leu583HisfsTer11) c.1720_1738dup (p.Leu580HisfsTer11) c.1630_1648dup (p.Leu550HisfsTer11) n.2191_2209dup | gnomAD v4 |
| 1 | g.156876502T>A | CA342938598 | NTRK1 | c.1555T>A (p.Cys519Ser) c.*327T>A (n.*327T>A) c.1735T>A (p.Cys579Ser) c.1726T>A (p.Cys576Ser) c.1717T>A (p.Cys573Ser) c.1627T>A (p.Cys543Ser) n.2188T>A | dbSNP |
| 1 | g.156876502T>C | CA342938599 | NTRK1 | c.1555T>C (p.Cys519Arg) c.*327T>C (n.*327T>C) c.1735T>C (p.Cys579Arg) c.1726T>C (p.Cys576Arg) c.1717T>C (p.Cys573Arg) c.1627T>C (p.Cys543Arg) n.2188T>C | dbSNP |
| 1 | g.156876502T>G | CA342938600 | NTRK1 | c.1555T>G (p.Cys519Gly) c.*327T>G (n.*327T>G) c.1735T>G (p.Cys579Gly) c.1726T>G (p.Cys576Gly) c.1717T>G (p.Cys573Gly) c.1627T>G (p.Cys543Gly) n.2188T>G | dbSNP |
| 1 | g.156876505_156876544del | CA2580061232 | NTRK1 | c.1558_1597del (p.Thr520GlyfsTer?) c.*330_*369del (n.*330_*369del) c.1738_1777del (p.Thr580GlyfsTer?) c.1729_1768del (p.Thr577GlyfsTer?) c.1720_1759del (p.Thr574GlyfsTer?) c.1630_1669del (p.Thr544GlyfsTer?) n.2191_2230del | ClinVar |
| 1 | g.156876503G>A | CA342938601 | NTRK1 | c.1556G>A (p.Cys519Tyr) c.*328G>A (n.*328G>A) c.1736G>A (p.Cys579Tyr) c.1727G>A (p.Cys576Tyr) c.1718G>A (p.Cys573Tyr) c.1628G>A (p.Cys543Tyr) n.2189G>A | dbSNP |
| 1 | g.156876503G>C | CA342938602 | NTRK1 | c.1556G>C (p.Cys519Ser) c.*328G>C (n.*328G>C) c.1736G>C (p.Cys579Ser) c.1727G>C (p.Cys576Ser) c.1718G>C (p.Cys573Ser) c.1628G>C (p.Cys543Ser) n.2189G>C | dbSNP |
| 1 | g.156876503G>T | CA342938603 | NTRK1 | c.1556G>T (p.Cys519Phe) c.*328G>T (n.*328G>T) c.1736G>T (p.Cys579Phe) c.1727G>T (p.Cys576Phe) c.1718G>T (p.Cys573Phe) c.1628G>T (p.Cys543Phe) n.2189G>T | |
| 1 | g.156876504C>A | CA342938605 | NTRK1 | c.1557C>A (p.Cys519Ter) c.*329C>A (n.*329C>A) c.1737C>A (p.Cys579Ter) c.1728C>A (p.Cys576Ter) c.1719C>A (p.Cys573Ter) c.1629C>A (p.Cys543Ter) n.2190C>A | dbSNP |
| 1 | g.156876504C>G | CA342938604 | NTRK1 | c.1557C>G (p.Cys519Trp) c.*329C>G (n.*329C>G) c.1737C>G (p.Cys579Trp) c.1728C>G (p.Cys576Trp) c.1719C>G (p.Cys573Trp) c.1629C>G (p.Cys543Trp) n.2190C>G | dbSNP |
| 1 | g.156876504C>T | CA421138889 | NTRK1 | c.1557C>T (p.Cys519=) c.*329C>T (n.*329C>T) c.1737C>T (p.Cys579=) c.1728C>T (p.Cys576=) c.1719C>T (p.Cys573=) c.1629C>T (p.Cys543=) n.2190C>T | ClinVar dbSNP |
| 1 | g.156876505A= | CA1200786128 | NTRK1 | c.1558A= (p.Thr520=) c.*330A= (n.*330A=) c.1738A= (p.Thr580=) c.1729A= (p.Thr577=) c.1720A= (p.Thr574=) c.1630A= (p.Thr544=) n.2191A= | |
| 1 | g.156876505A>C | CA342938606 | NTRK1 | c.1558A>C (p.Thr520Pro) c.*330A>C (n.*330A>C) c.1738A>C (p.Thr580Pro) c.1729A>C (p.Thr577Pro) c.1720A>C (p.Thr574Pro) c.1630A>C (p.Thr544Pro) n.2191A>C | dbSNP |
| 1 | g.156876505A>G | CA342938607 | NTRK1 | c.1558A>G (p.Thr520Ala) c.*330A>G (n.*330A>G) c.1738A>G (p.Thr580Ala) c.1729A>G (p.Thr577Ala) c.1720A>G (p.Thr574Ala) c.1630A>G (p.Thr544Ala) n.2191A>G | |
| 1 | g.156876505A>T | CA1169453 | NTRK1 | c.1558A>T (p.Thr520Ser) c.*330A>T (n.*330A>T) c.1738A>T (p.Thr580Ser) c.1729A>T (p.Thr577Ser) c.1720A>T (p.Thr574Ser) c.1630A>T (p.Thr544Ser) n.2191A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876506C>A | CA342938608 | NTRK1 | c.1559C>A (p.Thr520Asn) c.*331C>A (n.*331C>A) c.1739C>A (p.Thr580Asn) c.1730C>A (p.Thr577Asn) c.1721C>A (p.Thr574Asn) c.1631C>A (p.Thr544Asn) n.2192C>A | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876506C= | CA1200786129 | NTRK1 | c.1559C= (p.Thr520=) c.*331C= (n.*331C=) c.1739C= (p.Thr580=) c.1730C= (p.Thr577=) c.1721C= (p.Thr574=) c.1631C= (p.Thr544=) n.2192C= | |
| 1 | g.156876506C>G | CA1169454 | NTRK1 | c.1559C>G (p.Thr520Ser) c.*331C>G (n.*331C>G) c.1739C>G (p.Thr580Ser) c.1730C>G (p.Thr577Ser) c.1721C>G (p.Thr574Ser) c.1631C>G (p.Thr544Ser) n.2192C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156876506C>T | CA342938609 | NTRK1 | c.1559C>T (p.Thr520Ile) c.*331C>T (n.*331C>T) c.1739C>T (p.Thr580Ile) c.1730C>T (p.Thr577Ile) c.1721C>T (p.Thr574Ile) c.1631C>T (p.Thr544Ile) n.2192C>T | dbSNP |
| 1 | g.156876507C>A | CA421138893 | NTRK1 | c.1560C>A (p.Thr520=) c.*332C>A (n.*332C>A) c.1740C>A (p.Thr580=) c.1731C>A (p.Thr577=) c.1722C>A (p.Thr574=) c.1632C>A (p.Thr544=) n.2193C>A | dbSNP |
| 1 | g.156876507C= | CA1200786131 | NTRK1 | c.1560C= (p.Thr520=) c.*332C= (n.*332C=) c.1740C= (p.Thr580=) c.1731C= (p.Thr577=) c.1722C= (p.Thr574=) c.1632C= (p.Thr544=) n.2193C= | |
| 1 | g.156876507C>G | CA31118897 | NTRK1 | c.1560C>G (p.Thr520=) c.*332C>G (n.*332C>G) c.1740C>G (p.Thr580=) c.1731C>G (p.Thr577=) c.1722C>G (p.Thr574=) c.1632C>G (p.Thr544=) n.2193C>G | dbSNP |
| 1 | g.156876507C>T | CA421138896 | NTRK1 | c.1560C>T (p.Thr520=) c.*332C>T (n.*332C>T) c.1740C>T (p.Thr580=) c.1731C>T (p.Thr577=) c.1722C>T (p.Thr574=) c.1632C>T (p.Thr544=) n.2193C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156876507_156876508delinsCG | CA1200786130 | NTRK1 | c.1560_1561delinsCG (p.Thr520=) c.*332_*333delinsCG (n.*332_*333delinsCG) c.1740_1741delinsCG (p.Thr580=) c.1731_1732delinsCG (p.Thr577=) c.1722_1723delinsCG (p.Thr574=) c.1632_1633delinsCG (p.Thr544=) n.2193_2194delinsCG | |
| 1 | g.156876508del | CA1169455 | NTRK1 | c.1561del (p.Glu521ArgfsTer?) c.*333del (n.*333del) c.1741del (p.Glu581ArgfsTer?) c.1732del (p.Glu578ArgfsTer?) c.1723del (p.Glu575ArgfsTer?) c.1633del (p.Glu545ArgfsTer?) n.2194del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876508G>A | CA1169456 | NTRK1 | c.1561G>A (p.Glu521Lys) c.*333G>A (n.*333G>A) c.1741G>A (p.Glu581Lys) c.1732G>A (p.Glu578Lys) c.1723G>A (p.Glu575Lys) c.1633G>A (p.Glu545Lys) n.2194G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876508G>C | CA342938610 | NTRK1 | c.1561G>C (p.Glu521Gln) c.*333G>C (n.*333G>C) c.1741G>C (p.Glu581Gln) c.1732G>C (p.Glu578Gln) c.1723G>C (p.Glu575Gln) c.1633G>C (p.Glu545Gln) n.2194G>C | gnomAD v4 |
| 1 | g.156876508G= | CA1142373596 | NTRK1 | c.1561G= (p.Glu521=) c.*333G= (n.*333G=) c.1741G= (p.Glu581=) c.1732G= (p.Glu578=) c.1723G= (p.Glu575=) c.1633G= (p.Glu545=) n.2194G= | |
| 1 | g.156876508G>T | CA342938611 | NTRK1 | c.1561G>T (p.Glu521Ter) c.*333G>T (n.*333G>T) c.1741G>T (p.Glu581Ter) c.1732G>T (p.Glu578Ter) c.1723G>T (p.Glu575Ter) c.1633G>T (p.Glu545Ter) n.2194G>T | ClinVar |
| 1 | g.156876509A= | CA1200786132 | NTRK1 | c.1562A= (p.Glu521=) c.*334A= (n.*334A=) c.1742A= (p.Glu581=) c.1733A= (p.Glu578=) c.1724A= (p.Glu575=) c.1634A= (p.Glu545=) n.2195A= | |
| 1 | g.156876509A>C | CA342938612 | NTRK1 | c.1562A>C (p.Glu521Ala) c.*334A>C (n.*334A>C) c.1742A>C (p.Glu581Ala) c.1733A>C (p.Glu578Ala) c.1724A>C (p.Glu575Ala) c.1634A>C (p.Glu545Ala) n.2195A>C | |
| 1 | g.156876509A>G | CA1169457 | NTRK1 | c.1562A>G (p.Glu521Gly) c.*334A>G (n.*334A>G) c.1742A>G (p.Glu581Gly) c.1733A>G (p.Glu578Gly) c.1724A>G (p.Glu575Gly) c.1634A>G (p.Glu545Gly) n.2195A>G | ClinVar dbSNP ExAC gnomAD v2 |
| 1 | g.156876509A>T | CA342938613 | NTRK1 | c.1562A>T (p.Glu521Val) c.*334A>T (n.*334A>T) c.1742A>T (p.Glu581Val) c.1733A>T (p.Glu578Val) c.1724A>T (p.Glu575Val) c.1634A>T (p.Glu545Val) n.2195A>T | dbSNP |
| 1 | g.156876510G>A | CA31118928 | NTRK1 | c.1563G>A (p.Glu521=) c.*335G>A (n.*335G>A) c.1743G>A (p.Glu581=) c.1734G>A (p.Glu578=) c.1725G>A (p.Glu575=) c.1635G>A (p.Glu545=) n.2196G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 1 | g.156876510G>C | CA1169458 | NTRK1 | c.1563G>C (p.Glu521Asp) c.*335G>C (n.*335G>C) c.1743G>C (p.Glu581Asp) c.1734G>C (p.Glu578Asp) c.1725G>C (p.Glu575Asp) c.1635G>C (p.Glu545Asp) n.2196G>C | dbSNP ExAC gnomAD v2 |
| 1 | g.156876510G= | CA1141617035 | NTRK1 | c.1563G= (p.Glu521=) c.*335G= (n.*335G=) c.1743G= (p.Glu581=) c.1734G= (p.Glu578=) c.1725G= (p.Glu575=) c.1635G= (p.Glu545=) n.2196G= | |
| 1 | g.156876510G>T | CA342938614 | NTRK1 | c.1563G>T (p.Glu521Asp) c.*335G>T (n.*335G>T) c.1743G>T (p.Glu581Asp) c.1734G>T (p.Glu578Asp) c.1725G>T (p.Glu575Asp) c.1635G>T (p.Glu545Asp) n.2196G>T | dbSNP |
| 1 | g.156876511G>A | CA342938615 | NTRK1 | c.1564G>A (p.Gly522Ser) c.*336G>A (n.*336G>A) c.1744G>A (p.Gly582Ser) c.1735G>A (p.Gly579Ser) c.1726G>A (p.Gly576Ser) c.1636G>A (p.Gly546Ser) n.2197G>A | dbSNP gnomAD v4 |
| 1 | g.156876511G>C | CA342938617 | NTRK1 | c.1564G>C (p.Gly522Arg) c.*336G>C (n.*336G>C) c.1744G>C (p.Gly582Arg) c.1735G>C (p.Gly579Arg) c.1726G>C (p.Gly576Arg) c.1636G>C (p.Gly546Arg) n.2197G>C | dbSNP gnomAD v4 |
| 1 | g.156876511G>T | CA342938616 | NTRK1 | c.1564G>T (p.Gly522Cys) c.*336G>T (n.*336G>T) c.1744G>T (p.Gly582Cys) c.1735G>T (p.Gly579Cys) c.1726G>T (p.Gly576Cys) c.1636G>T (p.Gly546Cys) n.2197G>T | dbSNP |
| 1 | g.156876512G>A | CA342938618 | NTRK1 | c.1565G>A (p.Gly522Asp) c.*337G>A (n.*337G>A) c.1745G>A (p.Gly582Asp) c.1736G>A (p.Gly579Asp) c.1727G>A (p.Gly576Asp) c.1637G>A (p.Gly546Asp) n.2198G>A | dbSNP gnomAD v4 |
| 1 | g.156876512G>C | CA342938619 | NTRK1 | c.1565G>C (p.Gly522Ala) c.*337G>C (n.*337G>C) c.1745G>C (p.Gly582Ala) c.1736G>C (p.Gly579Ala) c.1727G>C (p.Gly576Ala) c.1637G>C (p.Gly546Ala) n.2198G>C | dbSNP |
| 1 | g.156876512G>T | CA342938620 | NTRK1 | c.1565G>T (p.Gly522Val) c.*337G>T (n.*337G>T) c.1745G>T (p.Gly582Val) c.1736G>T (p.Gly579Val) c.1727G>T (p.Gly576Val) c.1637G>T (p.Gly546Val) n.2198G>T | dbSNP |
| 1 | g.156876513C>A | CA31118939 | NTRK1 | c.1566C>A (p.Gly522=) c.*338C>A (n.*338C>A) c.1746C>A (p.Gly582=) c.1737C>A (p.Gly579=) c.1728C>A (p.Gly576=) c.1638C>A (p.Gly546=) n.2199C>A | ClinVar dbSNP gnomAD v4 |
| 1 | g.156876513C= | CA1200786133 | NTRK1 | c.1566C= (p.Gly522=) c.*338C= (n.*338C=) c.1746C= (p.Gly582=) c.1737C= (p.Gly579=) c.1728C= (p.Gly576=) c.1638C= (p.Gly546=) n.2199C= | |
| 1 | g.156876513C>G | CA421138921 | NTRK1 | c.1566C>G (p.Gly522=) c.*338C>G (n.*338C>G) c.1746C>G (p.Gly582=) c.1737C>G (p.Gly579=) c.1728C>G (p.Gly576=) c.1638C>G (p.Gly546=) n.2199C>G | dbSNP |
| 1 | g.156876513C>T | CA421138918 | NTRK1 | c.1566C>T (p.Gly522=) c.*338C>T (n.*338C>T) c.1746C>T (p.Gly582=) c.1737C>T (p.Gly579=) c.1728C>T (p.Gly576=) c.1638C>T (p.Gly546=) n.2199C>T | dbSNP |
| 1 | g.156876514C>A | CA342938621 | NTRK1 | c.1567C>A (p.Arg523Ser) c.*339C>A (n.*339C>A) c.1747C>A (p.Arg583Ser) c.1738C>A (p.Arg580Ser) c.1729C>A (p.Arg577Ser) c.1639C>A (p.Arg547Ser) n.2200C>A | dbSNP |
| 1 | g.156876514C= | CA1143789282 | NTRK1 | c.1567C= (p.Arg523=) c.*339C= (n.*339C=) c.1747C= (p.Arg583=) c.1738C= (p.Arg580=) c.1729C= (p.Arg577=) c.1639C= (p.Arg547=) n.2200C= | |
| 1 | g.156876514C>G | CA1169460 | NTRK1 | c.1567C>G (p.Arg523Gly) c.*339C>G (n.*339C>G) c.1747C>G (p.Arg583Gly) c.1738C>G (p.Arg580Gly) c.1729C>G (p.Arg577Gly) c.1639C>G (p.Arg547Gly) n.2200C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.156876514C>T | CA1169459 | NTRK1 | c.1567C>T (p.Arg523Cys) c.*339C>T (n.*339C>T) c.1747C>T (p.Arg583Cys) c.1738C>T (p.Arg580Cys) c.1729C>T (p.Arg577Cys) c.1639C>T (p.Arg547Cys) n.2200C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876515G>A | CA342938622 | NTRK1 | c.1568G>A (p.Arg523His) c.*340G>A (n.*340G>A) c.1748G>A (p.Arg583His) c.1739G>A (p.Arg580His) c.1730G>A (p.Arg577His) c.1640G>A (p.Arg547His) n.2201G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876515G>C | CA342938623 | NTRK1 | c.1568G>C (p.Arg523Pro) c.*340G>C (n.*340G>C) c.1748G>C (p.Arg583Pro) c.1739G>C (p.Arg580Pro) c.1730G>C (p.Arg577Pro) c.1640G>C (p.Arg547Pro) n.2201G>C | |
| 1 | g.156876515G= | CA1200786134 | NTRK1 | c.1568G= (p.Arg523=) c.*340G= (n.*340G=) c.1748G= (p.Arg583=) c.1739G= (p.Arg580=) c.1730G= (p.Arg577=) c.1640G= (p.Arg547=) n.2201G= | |
| 1 | g.156876515G>T | CA1169461 | NTRK1 | c.1568G>T (p.Arg523Leu) c.*340G>T (n.*340G>T) c.1748G>T (p.Arg583Leu) c.1739G>T (p.Arg580Leu) c.1730G>T (p.Arg577Leu) c.1640G>T (p.Arg547Leu) n.2201G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156876515_156876517delinsGCC | CA1200786135 | NTRK1 | c.1568_1570delinsGCC (p.Arg523=) c.*340_*342delinsGCC (n.*340_*342delinsGCC) c.1748_1750delinsGCC (p.Arg583=) c.1739_1741delinsGCC (p.Arg580=) c.1730_1732delinsGCC (p.Arg577=) c.1640_1642delinsGCC (p.Arg547=) n.2201_2203delinsGCC | |
| 1 | g.156876516C>A | CA421138931 | NTRK1 | c.1569C>A (p.Arg523=) c.*341C>A (n.*341C>A) c.1749C>A (p.Arg583=) c.1740C>A (p.Arg580=) c.1731C>A (p.Arg577=) c.1641C>A (p.Arg547=) n.2202C>A | |
| 1 | g.156876516C>G | CA421138933 | NTRK1 | c.1569C>G (p.Arg523=) c.*341C>G (n.*341C>G) c.1749C>G (p.Arg583=) c.1740C>G (p.Arg580=) c.1731C>G (p.Arg577=) c.1641C>G (p.Arg547=) n.2202C>G | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156876516C>T | CA421138936 | NTRK1 | c.1569C>T (p.Arg523=) c.*341C>T (n.*341C>T) c.1749C>T (p.Arg583=) c.1740C>T (p.Arg580=) c.1731C>T (p.Arg577=) c.1641C>T (p.Arg547=) n.2202C>T | dbSNP |
| 1 | g.156876516_156876520delinsCCCCC | CA1143389834 | NTRK1 | c.1569_1573delinsCCCCC (p.Arg523=) c.*341_*345delinsCCCCC (n.*341_*345delinsCCCCC) c.1749_1753delinsCCCCC (p.Arg583=) c.1740_1744delinsCCCCC (p.Arg580=) c.1731_1735delinsCCCCC (p.Arg577=) c.1641_1645delinsCCCCC (p.Arg547=) n.2202_2206delinsCCCCC | |
| 1 | g.156876520dup | CA2648464351 | NTRK1 | c.1573dup (p.Leu525ProfsTer6) c.*345dup (n.*345dup) c.1753dup (p.Leu585ProfsTer6) c.1744dup (p.Leu582ProfsTer6) c.1735dup (p.Leu579ProfsTer6) c.1645dup (p.Leu549ProfsTer6) n.2206dup | gnomAD v4 |
| 1 | g.156876520del | CA645518201 | NTRK1 | c.1573del (p.Leu525CysfsTer?) c.*345del (n.*345del) c.1753del (p.Leu585CysfsTer?) c.1744del (p.Leu582CysfsTer?) c.1735del (p.Leu579CysfsTer?) c.1645del (p.Leu549CysfsTer?) n.2206del | dbSNP gnomAD v4 COSMIC COSMIC |
| 1 | g.156876519_156876520del | CA31118982 | NTRK1 | c.1572_1573del (p.Leu525AlafsTer5) c.*344_*345del (n.*344_*345del) c.1752_1753del (p.Leu585AlafsTer5) c.1743_1744del (p.Leu582AlafsTer5) c.1734_1735del (p.Leu579AlafsTer5) c.1644_1645del (p.Leu549AlafsTer5) n.2205_2206del | dbSNP |
| 1 | g.156876517C>A | CA342938626 | NTRK1 | c.1570C>A (p.Pro524Thr) c.*342C>A (n.*342C>A) c.1750C>A (p.Pro584Thr) c.1741C>A (p.Pro581Thr) c.1732C>A (p.Pro578Thr) c.1642C>A (p.Pro548Thr) n.2203C>A | dbSNP |
| 1 | g.156876517C>G | CA342938625 | NTRK1 | c.1570C>G (p.Pro524Ala) c.*342C>G (n.*342C>G) c.1750C>G (p.Pro584Ala) c.1741C>G (p.Pro581Ala) c.1732C>G (p.Pro578Ala) c.1642C>G (p.Pro548Ala) n.2203C>G | dbSNP |
| 1 | g.156876517C>T | CA342938624 | NTRK1 | c.1570C>T (p.Pro524Ser) c.*342C>T (n.*342C>T) c.1750C>T (p.Pro584Ser) c.1741C>T (p.Pro581Ser) c.1732C>T (p.Pro578Ser) c.1642C>T (p.Pro548Ser) n.2203C>T | dbSNP |
| 1 | g.156876518C>A | CA342938627 | NTRK1 | c.1571C>A (p.Pro524His) c.*343C>A (n.*343C>A) c.1751C>A (p.Pro584His) c.1742C>A (p.Pro581His) c.1733C>A (p.Pro578His) c.1643C>A (p.Pro548His) n.2204C>A | dbSNP |
| 1 | g.156876518C>G | CA342938628 | NTRK1 | c.1571C>G (p.Pro524Arg) c.*343C>G (n.*343C>G) c.1751C>G (p.Pro584Arg) c.1742C>G (p.Pro581Arg) c.1733C>G (p.Pro578Arg) c.1643C>G (p.Pro548Arg) n.2204C>G | dbSNP |
| 1 | g.156876518C>T | CA342938629 | NTRK1 | c.1571C>T (p.Pro524Leu) c.*343C>T (n.*343C>T) c.1751C>T (p.Pro584Leu) c.1742C>T (p.Pro581Leu) c.1733C>T (p.Pro578Leu) c.1643C>T (p.Pro548Leu) n.2204C>T | dbSNP |
| 1 | g.156876519C>A | CA1169462 | NTRK1 | c.1572C>A (p.Pro524=) c.*344C>A (n.*344C>A) c.1752C>A (p.Pro584=) c.1743C>A (p.Pro581=) c.1734C>A (p.Pro578=) c.1644C>A (p.Pro548=) n.2205C>A | ClinVar dbSNP ExAC gnomAD v2 |
| 1 | g.156876519C= | CA1200786136 | NTRK1 | c.1572C= (p.Pro524=) c.*344C= (n.*344C=) c.1752C= (p.Pro584=) c.1743C= (p.Pro581=) c.1734C= (p.Pro578=) c.1644C= (p.Pro548=) n.2205C= | |
| 1 | g.156876519C>G | CA421138951 | NTRK1 | c.1572C>G (p.Pro524=) c.*344C>G (n.*344C>G) c.1752C>G (p.Pro584=) c.1743C>G (p.Pro581=) c.1734C>G (p.Pro578=) c.1644C>G (p.Pro548=) n.2205C>G | ClinVar dbSNP gnomAD v2 |
| 1 | g.156876519C>T | CA31119002 | NTRK1 | c.1572C>T (p.Pro524=) c.*344C>T (n.*344C>T) c.1752C>T (p.Pro584=) c.1743C>T (p.Pro581=) c.1734C>T (p.Pro578=) c.1644C>T (p.Pro548=) n.2205C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |