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 |
|---|---|---|---|---|---|
| 16 | g.89935045G>A | CA497381443 | TUBB3 | c.594G>A (p.Glu198=) n.4015G>A c.378G>A (p.Glu126=) c.277+1467G>A (n.277+1467G>A) c.*679G>A (n.*679G>A) c.*393G>A (n.*393G>A) c.1635G>A (p.Glu545=) | COSMIC |
| 16 | g.89935045G>C | CA397474912 | TUBB3 | c.594G>C (p.Glu198Asp) n.4015G>C c.378G>C (p.Glu126Asp) c.277+1467G>C (n.277+1467G>C) c.*679G>C (n.*679G>C) c.*393G>C (n.*393G>C) c.1635G>C (p.Glu545Asp) | |
| 16 | g.89935045G>T | CA397474913 | TUBB3 | c.594G>T (p.Glu198Asp) n.4015G>T c.378G>T (p.Glu126Asp) c.277+1467G>T (n.277+1467G>T) c.*679G>T (n.*679G>T) c.*393G>T (n.*393G>T) c.1635G>T (p.Glu545Asp) | dbSNP |
| 16 | g.89935046A= | CA2242019833 | TUBB3 | c.595A= (p.Thr199=) n.4016A= c.379A= (p.Thr127=) c.277+1468A= (n.277+1468A=) c.*680A= (n.*680A=) c.*394A= (n.*394A=) c.1636A= (p.Thr546=) | |
| 16 | g.89935046A>C | CA397474914 | TUBB3 | c.595A>C (p.Thr199Pro) n.4016A>C c.379A>C (p.Thr127Pro) c.277+1468A>C (n.277+1468A>C) c.*680A>C (n.*680A>C) c.*394A>C (n.*394A>C) c.1636A>C (p.Thr546Pro) | dbSNP |
| 16 | g.89935046A>G | CA397474915 | TUBB3 | c.595A>G (p.Thr199Ala) n.4016A>G c.379A>G (p.Thr127Ala) c.277+1468A>G (n.277+1468A>G) c.*680A>G (n.*680A>G) c.*394A>G (n.*394A>G) c.1636A>G (p.Thr546Ala) | |
| 16 | g.89935046A>T | CA397474916 | TUBB3 | c.595A>T (p.Thr199Ser) n.4016A>T c.379A>T (p.Thr127Ser) c.277+1468A>T (n.277+1468A>T) c.*680A>T (n.*680A>T) c.*394A>T (n.*394A>T) c.1636A>T (p.Thr546Ser) | |
| 16 | g.89935047C>A | CA397474917 | TUBB3 | c.596C>A (p.Thr199Asn) n.4017C>A c.380C>A (p.Thr127Asn) c.277+1469C>A (n.277+1469C>A) c.*681C>A (n.*681C>A) c.*395C>A (n.*395C>A) c.1637C>A (p.Thr546Asn) | |
| 16 | g.89935047C= | CA2242019837 | TUBB3 | c.596C= (p.Thr199=) n.4017C= c.380C= (p.Thr127=) c.277+1469C= (n.277+1469C=) c.*681C= (n.*681C=) c.*395C= (n.*395C=) c.1637C= (p.Thr546=) | |
| 16 | g.89935047C>G | CA397474918 | TUBB3 | c.596C>G (p.Thr199Ser) n.4017C>G c.380C>G (p.Thr127Ser) c.277+1469C>G (n.277+1469C>G) c.*681C>G (n.*681C>G) c.*395C>G (n.*395C>G) c.1637C>G (p.Thr546Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89935047C>T | CA397474919 | TUBB3 | c.596C>T (p.Thr199Ile) n.4017C>T c.380C>T (p.Thr127Ile) c.277+1469C>T (n.277+1469C>T) c.*681C>T (n.*681C>T) c.*395C>T (n.*395C>T) c.1637C>T (p.Thr546Ile) | ClinVar |
| 16 | g.89935048C>A | CA497381444 | TUBB3 | c.597C>A (p.Thr199=) n.4018C>A c.381C>A (p.Thr127=) c.277+1470C>A (n.277+1470C>A) c.*682C>A (n.*682C>A) c.*396C>A (n.*396C>A) c.1638C>A (p.Thr546=) | |
| 16 | g.89935048C= | CA2242019839 | TUBB3 | c.597C= (p.Thr199=) n.4018C= c.381C= (p.Thr127=) c.277+1470C= (n.277+1470C=) c.*682C= (n.*682C=) c.*396C= (n.*396C=) c.1638C= (p.Thr546=) | |
| 16 | g.89935048C>G | CA8256134 | TUBB3 | c.597C>G (p.Thr199=) n.4018C>G c.381C>G (p.Thr127=) c.277+1470C>G (n.277+1470C>G) c.*682C>G (n.*682C>G) c.*396C>G (n.*396C>G) c.1638C>G (p.Thr546=) | dbSNP ExAC gnomAD v4 |
| 16 | g.89935048C>T | CA497381445 | TUBB3 | c.597C>T (p.Thr199=) n.4018C>T c.381C>T (p.Thr127=) c.277+1470C>T (n.277+1470C>T) c.*682C>T (n.*682C>T) c.*396C>T (n.*396C>T) c.1638C>T (p.Thr546=) | gnomAD v4 |
| 16 | g.89935049T>A | CA397474922 | TUBB3 | c.598T>A (p.Tyr200Asn) n.4019T>A c.382T>A (p.Tyr128Asn) c.277+1471T>A (n.277+1471T>A) c.*683T>A (n.*683T>A) c.*397T>A (n.*397T>A) c.1639T>A (p.Tyr547Asn) | |
| 16 | g.89935049T>C | CA397474920 | TUBB3 | c.598T>C (p.Tyr200His) n.4019T>C c.382T>C (p.Tyr128His) c.277+1471T>C (n.277+1471T>C) c.*683T>C (n.*683T>C) c.*397T>C (n.*397T>C) c.1639T>C (p.Tyr547His) | |
| 16 | g.89935049T>G | CA397474921 | TUBB3 | c.598T>G (p.Tyr200Asp) n.4019T>G c.382T>G (p.Tyr128Asp) c.277+1471T>G (n.277+1471T>G) c.*683T>G (n.*683T>G) c.*397T>G (n.*397T>G) c.1639T>G (p.Tyr547Asp) | |
| 16 | g.89935050A= | CA2242019844 | TUBB3 | c.599A= (p.Tyr200=) n.4020A= c.383A= (p.Tyr128=) c.277+1472A= (n.277+1472A=) c.*684A= (n.*684A=) c.*398A= (n.*398A=) c.1640A= (p.Tyr547=) | |
| 16 | g.89935050A>C | CA397474923 | TUBB3 | c.599A>C (p.Tyr200Ser) n.4020A>C c.383A>C (p.Tyr128Ser) c.277+1472A>C (n.277+1472A>C) c.*684A>C (n.*684A>C) c.*398A>C (n.*398A>C) c.1640A>C (p.Tyr547Ser) | |
| 16 | g.89935050A>G | CA397474924 | TUBB3 | c.599A>G (p.Tyr200Cys) n.4020A>G c.383A>G (p.Tyr128Cys) c.277+1472A>G (n.277+1472A>G) c.*684A>G (n.*684A>G) c.*398A>G (n.*398A>G) c.1640A>G (p.Tyr547Cys) | |
| 16 | g.89935050A>T | CA397474925 | TUBB3 | c.599A>T (p.Tyr200Phe) n.4020A>T c.383A>T (p.Tyr128Phe) c.277+1472A>T (n.277+1472A>T) c.*684A>T (n.*684A>T) c.*398A>T (n.*398A>T) c.1640A>T (p.Tyr547Phe) | dbSNP |
| 16 | g.89935051C>A | CA397474926 | TUBB3 | c.600C>A (p.Tyr200Ter) n.4021C>A c.384C>A (p.Tyr128Ter) c.277+1473C>A (n.277+1473C>A) c.*685C>A (n.*685C>A) c.*399C>A (n.*399C>A) c.1641C>A (p.Tyr547Ter) | |
| 16 | g.89935051C>G | CA397474927 | TUBB3 | c.600C>G (p.Tyr200Ter) n.4021C>G c.384C>G (p.Tyr128Ter) c.277+1473C>G (n.277+1473C>G) c.*685C>G (n.*685C>G) c.*399C>G (n.*399C>G) c.1641C>G (p.Tyr547Ter) | COSMIC |
| 16 | g.89935051C>T | CA497381446 | TUBB3 | c.600C>T (p.Tyr200=) n.4021C>T c.384C>T (p.Tyr128=) c.277+1473C>T (n.277+1473C>T) c.*685C>T (n.*685C>T) c.*399C>T (n.*399C>T) c.1641C>T (p.Tyr547=) | |
| 16 | g.89935052T>A | CA397474928 | TUBB3 | c.601T>A (p.Cys201Ser) n.4022T>A c.385T>A (p.Cys129Ser) c.277+1474T>A (n.277+1474T>A) c.*686T>A (n.*686T>A) c.*400T>A (n.*400T>A) c.1642T>A (p.Cys548Ser) | |
| 16 | g.89935052T>C | CA397474929 | TUBB3 | c.601T>C (p.Cys201Arg) n.4022T>C c.385T>C (p.Cys129Arg) c.277+1474T>C (n.277+1474T>C) c.*686T>C (n.*686T>C) c.*400T>C (n.*400T>C) c.1642T>C (p.Cys548Arg) | |
| 16 | g.89935052T>G | CA397474930 | TUBB3 | c.601T>G (p.Cys201Gly) n.4022T>G c.385T>G (p.Cys129Gly) c.277+1474T>G (n.277+1474T>G) c.*686T>G (n.*686T>G) c.*400T>G (n.*400T>G) c.1642T>G (p.Cys548Gly) | |
| 16 | g.89935053G>A | CA397474931 | TUBB3 | c.602G>A (p.Cys201Tyr) n.4023G>A c.386G>A (p.Cys129Tyr) c.277+1475G>A (n.277+1475G>A) c.*687G>A (n.*687G>A) c.*401G>A (n.*401G>A) c.1643G>A (p.Cys548Tyr) | |
| 16 | g.89935053G>C | CA397474932 | TUBB3 | c.602G>C (p.Cys201Ser) n.4023G>C c.386G>C (p.Cys129Ser) c.277+1475G>C (n.277+1475G>C) c.*687G>C (n.*687G>C) c.*401G>C (n.*401G>C) c.1643G>C (p.Cys548Ser) | |
| 16 | g.89935053G>T | CA397474933 | TUBB3 | c.602G>T (p.Cys201Phe) n.4023G>T c.386G>T (p.Cys129Phe) c.277+1475G>T (n.277+1475G>T) c.*687G>T (n.*687G>T) c.*401G>T (n.*401G>T) c.1643G>T (p.Cys548Phe) | |
| 16 | g.89935054C>A | CA397474935 | TUBB3 | c.603C>A (p.Cys201Ter) n.4024C>A c.387C>A (p.Cys129Ter) c.277+1476C>A (n.277+1476C>A) c.*688C>A (n.*688C>A) c.*402C>A (n.*402C>A) c.1644C>A (p.Cys548Ter) | |
| 16 | g.89935054C= | CA2242019846 | TUBB3 | c.603C= (p.Cys201=) n.4024C= c.387C= (p.Cys129=) c.277+1476C= (n.277+1476C=) c.*688C= (n.*688C=) c.*402C= (n.*402C=) c.1644C= (p.Cys548=) | |
| 16 | g.89935054C>G | CA397474934 | TUBB3 | c.603C>G (p.Cys201Trp) n.4024C>G c.387C>G (p.Cys129Trp) c.277+1476C>G (n.277+1476C>G) c.*688C>G (n.*688C>G) c.*402C>G (n.*402C>G) c.1644C>G (p.Cys548Trp) | |
| 16 | g.89935054C>T | CA497381447 | TUBB3 | c.603C>T (p.Cys201=) n.4024C>T c.387C>T (p.Cys129=) c.277+1476C>T (n.277+1476C>T) c.*688C>T (n.*688C>T) c.*402C>T (n.*402C>T) c.1644C>T (p.Cys548=) | dbSNP gnomAD v4 |
| 16 | g.89935055A>C | CA397474936 | TUBB3 | c.604A>C (p.Ile202Leu) n.4025A>C c.388A>C (p.Ile130Leu) c.277+1477A>C (n.277+1477A>C) c.*689A>C (n.*689A>C) c.*403A>C (n.*403A>C) c.1645A>C (p.Ile549Leu) | |
| 16 | g.89935055A>G | CA397474937 | TUBB3 | c.604A>G (p.Ile202Val) n.4025A>G c.388A>G (p.Ile130Val) c.277+1477A>G (n.277+1477A>G) c.*689A>G (n.*689A>G) c.*403A>G (n.*403A>G) c.1645A>G (p.Ile549Val) | |
| 16 | g.89935055A>T | CA397474938 | TUBB3 | c.604A>T (p.Ile202Phe) n.4025A>T c.388A>T (p.Ile130Phe) c.277+1477A>T (n.277+1477A>T) c.*689A>T (n.*689A>T) c.*403A>T (n.*403A>T) c.1645A>T (p.Ile549Phe) | |
| 16 | g.89935056T>A | CA397474939 | TUBB3 | c.605T>A (p.Ile202Asn) n.4026T>A c.389T>A (p.Ile130Asn) c.277+1478T>A (n.277+1478T>A) c.*690T>A (n.*690T>A) c.*404T>A (n.*404T>A) c.1646T>A (p.Ile549Asn) | |
| 16 | g.89935056T>C | CA397474940 | TUBB3 | c.605T>C (p.Ile202Thr) n.4026T>C c.389T>C (p.Ile130Thr) c.277+1478T>C (n.277+1478T>C) c.*690T>C (n.*690T>C) c.*404T>C (n.*404T>C) c.1646T>C (p.Ile549Thr) | |
| 16 | g.89935056T>G | CA397474941 | TUBB3 | c.605T>G (p.Ile202Ser) n.4026T>G c.389T>G (p.Ile130Ser) c.277+1478T>G (n.277+1478T>G) c.*690T>G (n.*690T>G) c.*404T>G (n.*404T>G) c.1646T>G (p.Ile549Ser) | |
| 16 | g.89935057C>A | CA497381448 | TUBB3 | c.606C>A (p.Ile202=) n.4027C>A c.390C>A (p.Ile130=) c.277+1479C>A (n.277+1479C>A) c.*691C>A (n.*691C>A) c.*405C>A (n.*405C>A) c.1647C>A (p.Ile549=) | |
| 16 | g.89935057C= | CA2242019849 | TUBB3 | c.606C= (p.Ile202=) n.4027C= c.390C= (p.Ile130=) c.277+1479C= (n.277+1479C=) c.*691C= (n.*691C=) c.*405C= (n.*405C=) c.1647C= (p.Ile549=) | |
| 16 | g.89935057C>G | CA397474942 | TUBB3 | c.606C>G (p.Ile202Met) n.4027C>G c.390C>G (p.Ile130Met) c.277+1479C>G (n.277+1479C>G) c.*691C>G (n.*691C>G) c.*405C>G (n.*405C>G) c.1647C>G (p.Ile549Met) | gnomAD v4 |
| 16 | g.89935057C>T | CA8256135 | TUBB3 | c.606C>T (p.Ile202=) n.4027C>T c.390C>T (p.Ile130=) c.277+1479C>T (n.277+1479C>T) c.*691C>T (n.*691C>T) c.*405C>T (n.*405C>T) c.1647C>T (p.Ile549=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935058G>A | CA397474943 | TUBB3 | c.607G>A (p.Asp203Asn) n.4028G>A c.391G>A (p.Asp131Asn) c.277+1480G>A (n.277+1480G>A) c.*692G>A (n.*692G>A) c.*406G>A (n.*406G>A) c.1648G>A (p.Asp550Asn) | |
| 16 | g.89935058G>C | CA397474944 | TUBB3 | c.607G>C (p.Asp203His) n.4028G>C c.391G>C (p.Asp131His) c.277+1480G>C (n.277+1480G>C) c.*692G>C (n.*692G>C) c.*406G>C (n.*406G>C) c.1648G>C (p.Asp550His) | |
| 16 | g.89935058G>T | CA397474945 | TUBB3 | c.607G>T (p.Asp203Tyr) n.4028G>T c.391G>T (p.Asp131Tyr) c.277+1480G>T (n.277+1480G>T) c.*692G>T (n.*692G>T) c.*406G>T (n.*406G>T) c.1648G>T (p.Asp550Tyr) | |
| 16 | g.89935059A>C | CA397474946 | TUBB3 | c.608A>C (p.Asp203Ala) n.4029A>C c.392A>C (p.Asp131Ala) c.277+1481A>C (n.277+1481A>C) c.*693A>C (n.*693A>C) c.*407A>C (n.*407A>C) c.1649A>C (p.Asp550Ala) | |
| 16 | g.89935059A>G | CA397474947 | TUBB3 | c.608A>G (p.Asp203Gly) n.4029A>G c.392A>G (p.Asp131Gly) c.277+1481A>G (n.277+1481A>G) c.*693A>G (n.*693A>G) c.*407A>G (n.*407A>G) c.1649A>G (p.Asp550Gly) | |
| 16 | g.89935059A>T | CA397474948 | TUBB3 | c.608A>T (p.Asp203Val) n.4029A>T c.392A>T (p.Asp131Val) c.277+1481A>T (n.277+1481A>T) c.*693A>T (n.*693A>T) c.*407A>T (n.*407A>T) c.1649A>T (p.Asp550Val) | |
| 16 | g.89935061_89935063del | CA2635070777 | TUBB3 | c.610_612del (p.Asn204del) n.4031_4033del c.394_396del (p.Asn132del) c.277+1483_277+1485del (n.277+1483_277+1485del) c.*695_*697del (n.*695_*697del) c.*409_*411del (n.*409_*411del) c.1651_1653del (p.Asn551del) | gnomAD v4 |
| 16 | g.89935060C>A | CA397474949 | TUBB3 | c.609C>A (p.Asp203Glu) n.4030C>A c.393C>A (p.Asp131Glu) c.277+1482C>A (n.277+1482C>A) c.*694C>A (n.*694C>A) c.*408C>A (n.*408C>A) c.1650C>A (p.Asp550Glu) | |
| 16 | g.89935060C= | CA2242019852 | TUBB3 | c.609C= (p.Asp203=) n.4030C= c.393C= (p.Asp131=) c.277+1482C= (n.277+1482C=) c.*694C= (n.*694C=) c.*408C= (n.*408C=) c.1650C= (p.Asp550=) | |
| 16 | g.89935060C>G | CA397474950 | TUBB3 | c.609C>G (p.Asp203Glu) n.4030C>G c.393C>G (p.Asp131Glu) c.277+1482C>G (n.277+1482C>G) c.*694C>G (n.*694C>G) c.*408C>G (n.*408C>G) c.1650C>G (p.Asp550Glu) | |
| 16 | g.89935060C>T | CA8256136 | TUBB3 | c.609C>T (p.Asp203=) n.4030C>T c.393C>T (p.Asp131=) c.277+1482C>T (n.277+1482C>T) c.*694C>T (n.*694C>T) c.*408C>T (n.*408C>T) c.1650C>T (p.Asp550=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935061A>C | CA397474951 | TUBB3 | c.610A>C (p.Asn204His) n.4031A>C c.394A>C (p.Asn132His) c.277+1483A>C (n.277+1483A>C) c.*695A>C (n.*695A>C) c.*409A>C (n.*409A>C) c.1651A>C (p.Asn551His) | |
| 16 | g.89935061A>G | CA397474952 | TUBB3 | c.610A>G (p.Asn204Asp) n.4031A>G c.394A>G (p.Asn132Asp) c.277+1483A>G (n.277+1483A>G) c.*695A>G (n.*695A>G) c.*409A>G (n.*409A>G) c.1651A>G (p.Asn551Asp) | |
| 16 | g.89935061A>T | CA397474953 | TUBB3 | c.610A>T (p.Asn204Tyr) n.4031A>T c.394A>T (p.Asn132Tyr) c.277+1483A>T (n.277+1483A>T) c.*695A>T (n.*695A>T) c.*409A>T (n.*409A>T) c.1651A>T (p.Asn551Tyr) | |
| 16 | g.89935062A>C | CA397474954 | TUBB3 | c.611A>C (p.Asn204Thr) n.4032A>C c.395A>C (p.Asn132Thr) c.277+1484A>C (n.277+1484A>C) c.*696A>C (n.*696A>C) c.*410A>C (n.*410A>C) c.1652A>C (p.Asn551Thr) | |
| 16 | g.89935062A>G | CA397474955 | TUBB3 | c.611A>G (p.Asn204Ser) n.4032A>G c.395A>G (p.Asn132Ser) c.277+1484A>G (n.277+1484A>G) c.*696A>G (n.*696A>G) c.*410A>G (n.*410A>G) c.1652A>G (p.Asn551Ser) | |
| 16 | g.89935062A>T | CA397474956 | TUBB3 | c.611A>T (p.Asn204Ile) n.4032A>T c.395A>T (p.Asn132Ile) c.277+1484A>T (n.277+1484A>T) c.*696A>T (n.*696A>T) c.*410A>T (n.*410A>T) c.1652A>T (p.Asn551Ile) | |
| 16 | g.89935063C>A | CA397474957 | TUBB3 | c.612C>A (p.Asn204Lys) n.4033C>A c.396C>A (p.Asn132Lys) c.277+1485C>A (n.277+1485C>A) c.*697C>A (n.*697C>A) c.*411C>A (n.*411C>A) c.1653C>A (p.Asn551Lys) | |
| 16 | g.89935063C= | CA2242019855 | TUBB3 | c.612C= (p.Asn204=) n.4033C= c.396C= (p.Asn132=) c.277+1485C= (n.277+1485C=) c.*697C= (n.*697C=) c.*411C= (n.*411C=) c.1653C= (p.Asn551=) | |
| 16 | g.89935063C>G | CA397474958 | TUBB3 | c.612C>G (p.Asn204Lys) n.4033C>G c.396C>G (p.Asn132Lys) c.277+1485C>G (n.277+1485C>G) c.*697C>G (n.*697C>G) c.*411C>G (n.*411C>G) c.1653C>G (p.Asn551Lys) | |
| 16 | g.89935063C>T | CA8256137 | TUBB3 | c.612C>T (p.Asn204=) n.4033C>T c.396C>T (p.Asn132=) c.277+1485C>T (n.277+1485C>T) c.*697C>T (n.*697C>T) c.*411C>T (n.*411C>T) c.1653C>T (p.Asn551=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935064G>A | CA10575549 | TUBB3 | c.613G>A (p.Glu205Lys) n.4034G>A c.397G>A (p.Glu133Lys) c.277+1486G>A (n.277+1486G>A) c.*698G>A (n.*698G>A) c.*412G>A (n.*412G>A) c.1654G>A (p.Glu552Lys) | ClinVar dbSNP COSMIC |
| 16 | g.89935064G>C | CA397474959 | TUBB3 | c.613G>C (p.Glu205Gln) n.4034G>C c.397G>C (p.Glu133Gln) c.277+1486G>C (n.277+1486G>C) c.*698G>C (n.*698G>C) c.*412G>C (n.*412G>C) c.1654G>C (p.Glu552Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935064G= | CA2242019858 | TUBB3 | c.613G= (p.Glu205=) n.4034G= c.397G= (p.Glu133=) c.277+1486G= (n.277+1486G=) c.*698G= (n.*698G=) c.*412G= (n.*412G=) c.1654G= (p.Glu552=) | |
| 16 | g.89935064G>T | CA397474960 | TUBB3 | c.613G>T (p.Glu205Ter) n.4034G>T c.397G>T (p.Glu133Ter) c.277+1486G>T (n.277+1486G>T) c.*698G>T (n.*698G>T) c.*412G>T (n.*412G>T) c.1654G>T (p.Glu552Ter) | |
| 16 | g.89935065A= | CA2242019867 | TUBB3 | c.614A= (p.Glu205=) n.4035A= c.398A= (p.Glu133=) c.277+1487A= (n.277+1487A=) c.*699A= (n.*699A=) c.*413A= (n.*413A=) c.1655A= (p.Glu552=) | |
| 16 | g.89935065A>C | CA16042959 | TUBB3 | c.614A>C (p.Glu205Ala) n.4035A>C c.398A>C (p.Glu133Ala) c.277+1487A>C (n.277+1487A>C) c.*699A>C (n.*699A>C) c.*413A>C (n.*413A>C) c.1655A>C (p.Glu552Ala) | ClinVar dbSNP |
| 16 | g.89935065A>G | CA397474961 | TUBB3 | c.614A>G (p.Glu205Gly) n.4035A>G c.398A>G (p.Glu133Gly) c.277+1487A>G (n.277+1487A>G) c.*699A>G (n.*699A>G) c.*413A>G (n.*413A>G) c.1655A>G (p.Glu552Gly) | |
| 16 | g.89935065A>T | CA397474962 | TUBB3 | c.614A>T (p.Glu205Val) n.4035A>T c.398A>T (p.Glu133Val) c.277+1487A>T (n.277+1487A>T) c.*699A>T (n.*699A>T) c.*413A>T (n.*413A>T) c.1655A>T (p.Glu552Val) | |
| 16 | g.89935066G>A | CA497381449 | TUBB3 | c.615G>A (p.Glu205=) n.4036G>A c.399G>A (p.Glu133=) c.277+1488G>A (n.277+1488G>A) c.*700G>A (n.*700G>A) c.*414G>A (n.*414G>A) c.1656G>A (p.Glu552=) | |
| 16 | g.89935066G>C | CA397474963 | TUBB3 | c.615G>C (p.Glu205Asp) n.4036G>C c.399G>C (p.Glu133Asp) c.277+1488G>C (n.277+1488G>C) c.*700G>C (n.*700G>C) c.*414G>C (n.*414G>C) c.1656G>C (p.Glu552Asp) | |
| 16 | g.89935066G>T | CA397474964 | TUBB3 | c.615G>T (p.Glu205Asp) n.4036G>T c.399G>T (p.Glu133Asp) c.277+1488G>T (n.277+1488G>T) c.*700G>T (n.*700G>T) c.*414G>T (n.*414G>T) c.1656G>T (p.Glu552Asp) | |
| 16 | g.89935067G>A | CA397474965 | TUBB3 | c.616G>A (p.Ala206Thr) n.4037G>A c.400G>A (p.Ala134Thr) c.277+1489G>A (n.277+1489G>A) c.*701G>A (n.*701G>A) c.*415G>A (n.*415G>A) c.1657G>A (p.Ala553Thr) | |
| 16 | g.89935067G>C | CA397474966 | TUBB3 | c.616G>C (p.Ala206Pro) n.4037G>C c.400G>C (p.Ala134Pro) c.277+1489G>C (n.277+1489G>C) c.*701G>C (n.*701G>C) c.*415G>C (n.*415G>C) c.1657G>C (p.Ala553Pro) | |
| 16 | g.89935067G>T | CA397474967 | TUBB3 | c.616G>T (p.Ala206Ser) n.4037G>T c.400G>T (p.Ala134Ser) c.277+1489G>T (n.277+1489G>T) c.*701G>T (n.*701G>T) c.*415G>T (n.*415G>T) c.1657G>T (p.Ala553Ser) | |
| 16 | g.89935068C>A | CA397474968 | TUBB3 | c.617C>A (p.Ala206Glu) n.4038C>A c.401C>A (p.Ala134Glu) c.277+1490C>A (n.277+1490C>A) c.*702C>A (n.*702C>A) c.*416C>A (n.*416C>A) c.1658C>A (p.Ala553Glu) | |
| 16 | g.89935068C= | CA2242019873 | TUBB3 | c.617C= (p.Ala206=) n.4038C= c.401C= (p.Ala134=) c.277+1490C= (n.277+1490C=) c.*702C= (n.*702C=) c.*416C= (n.*416C=) c.1658C= (p.Ala553=) | |
| 16 | g.89935068C>G | CA397474969 | TUBB3 | c.617C>G (p.Ala206Gly) n.4038C>G c.401C>G (p.Ala134Gly) c.277+1490C>G (n.277+1490C>G) c.*702C>G (n.*702C>G) c.*416C>G (n.*416C>G) c.1658C>G (p.Ala553Gly) | |
| 16 | g.89935068C>T | CA8256138 | TUBB3 | c.617C>T (p.Ala206Val) n.4038C>T c.401C>T (p.Ala134Val) c.277+1490C>T (n.277+1490C>T) c.*702C>T (n.*702C>T) c.*416C>T (n.*416C>T) c.1658C>T (p.Ala553Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935069G>A | CA8256139 | TUBB3 | c.618G>A (p.Ala206=) n.4039G>A c.402G>A (p.Ala134=) c.277+1491G>A (n.277+1491G>A) c.*703G>A (n.*703G>A) c.*417G>A (n.*417G>A) c.1659G>A (p.Ala553=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935069G>C | CA497381450 | TUBB3 | c.618G>C (p.Ala206=) n.4039G>C c.402G>C (p.Ala134=) c.277+1491G>C (n.277+1491G>C) c.*703G>C (n.*703G>C) c.*417G>C (n.*417G>C) c.1659G>C (p.Ala553=) | gnomAD v4 |
| 16 | g.89935069G= | CA2242019879 | TUBB3 | c.618G= (p.Ala206=) n.4039G= c.402G= (p.Ala134=) c.277+1491G= (n.277+1491G=) c.*703G= (n.*703G=) c.*417G= (n.*417G=) c.1659G= (p.Ala553=) | |
| 16 | g.89935069G>T | CA497381451 | TUBB3 | c.618G>T (p.Ala206=) n.4039G>T c.402G>T (p.Ala134=) c.277+1491G>T (n.277+1491G>T) c.*703G>T (n.*703G>T) c.*417G>T (n.*417G>T) c.1659G>T (p.Ala553=) | dbSNP gnomAD v4 |
| 16 | g.89935070C>A | CA397474970 | TUBB3 | c.619C>A (p.Leu207Ile) n.4040C>A c.403C>A (p.Leu135Ile) c.277+1492C>A (n.277+1492C>A) c.*704C>A (n.*704C>A) c.*418C>A (n.*418C>A) c.1660C>A (p.Leu554Ile) | |
| 16 | g.89935070C>G | CA397474971 | TUBB3 | c.619C>G (p.Leu207Val) n.4040C>G c.403C>G (p.Leu135Val) c.277+1492C>G (n.277+1492C>G) c.*704C>G (n.*704C>G) c.*418C>G (n.*418C>G) c.1660C>G (p.Leu554Val) | |
| 16 | g.89935070C>T | CA397474972 | TUBB3 | c.619C>T (p.Leu207Phe) n.4040C>T c.403C>T (p.Leu135Phe) c.277+1492C>T (n.277+1492C>T) c.*704C>T (n.*704C>T) c.*418C>T (n.*418C>T) c.1660C>T (p.Leu554Phe) | |
| 16 | g.89935071T>A | CA397474973 | TUBB3 | c.620T>A (p.Leu207His) n.4041T>A c.404T>A (p.Leu135His) c.277+1493T>A (n.277+1493T>A) c.*705T>A (n.*705T>A) c.1661T>A (p.Leu554His) | |
| 16 | g.89935071T>C | CA397474974 | TUBB3 | c.620T>C (p.Leu207Pro) n.4041T>C c.404T>C (p.Leu135Pro) c.277+1493T>C (n.277+1493T>C) c.*705T>C (n.*705T>C) c.1661T>C (p.Leu554Pro) | |
| 16 | g.89935071T>G | CA397474975 | TUBB3 | c.620T>G (p.Leu207Arg) n.4041T>G c.404T>G (p.Leu135Arg) c.277+1493T>G (n.277+1493T>G) c.*705T>G (n.*705T>G) c.1661T>G (p.Leu554Arg) | |
| 16 | g.89935072C>A | CA497381452 | TUBB3 | c.621C>A (p.Leu207=) n.4042C>A c.405C>A (p.Leu135=) c.277+1494C>A (n.277+1494C>A) c.*706C>A (n.*706C>A) c.1662C>A (p.Leu554=) | |
| 16 | g.89935072C= | CA2242019885 | TUBB3 | c.621C= (p.Leu207=) n.4042C= c.405C= (p.Leu135=) c.277+1494C= (n.277+1494C=) c.*706C= (n.*706C=) c.1662C= (p.Leu554=) | |
| 16 | g.89935072C>G | CA497381453 | TUBB3 | c.621C>G (p.Leu207=) n.4042C>G c.405C>G (p.Leu135=) c.277+1494C>G (n.277+1494C>G) c.*706C>G (n.*706C>G) c.1662C>G (p.Leu554=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935072C>T | CA497381454 | TUBB3 | c.621C>T (p.Leu207=) n.4042C>T c.405C>T (p.Leu135=) c.277+1494C>T (n.277+1494C>T) c.*706C>T (n.*706C>T) c.1662C>T (p.Leu554=) | |
| 16 | g.89935073T>A | CA397474978 | TUBB3 | c.622T>A (p.Tyr208Asn) n.4043T>A c.406T>A (p.Tyr136Asn) c.277+1495T>A (n.277+1495T>A) c.*707T>A (n.*707T>A) c.1663T>A (p.Tyr555Asn) | |
| 16 | g.89935073T>C | CA397474976 | TUBB3 | c.622T>C (p.Tyr208His) n.4043T>C c.406T>C (p.Tyr136His) c.277+1495T>C (n.277+1495T>C) c.*707T>C (n.*707T>C) c.1663T>C (p.Tyr555His) | |
| 16 | g.89935073T>G | CA397474977 | TUBB3 | c.622T>G (p.Tyr208Asp) n.4043T>G c.406T>G (p.Tyr136Asp) c.277+1495T>G (n.277+1495T>G) c.*707T>G (n.*707T>G) c.1663T>G (p.Tyr555Asp) | |
| 16 | g.89935074A>C | CA397474979 | TUBB3 | c.623A>C (p.Tyr208Ser) n.4044A>C c.407A>C (p.Tyr136Ser) c.277+1496A>C (n.277+1496A>C) c.*708A>C (n.*708A>C) c.1664A>C (p.Tyr555Ser) | |
| 16 | g.89935074A>G | CA397474980 | TUBB3 | c.623A>G (p.Tyr208Cys) n.4044A>G c.407A>G (p.Tyr136Cys) c.277+1496A>G (n.277+1496A>G) c.*708A>G (n.*708A>G) c.1664A>G (p.Tyr555Cys) | |
| 16 | g.89935074A>T | CA397474981 | TUBB3 | c.623A>T (p.Tyr208Phe) n.4044A>T c.407A>T (p.Tyr136Phe) c.277+1496A>T (n.277+1496A>T) c.*708A>T (n.*708A>T) c.1664A>T (p.Tyr555Phe) | |
| 16 | g.89935075C>A | CA397474982 | TUBB3 | c.624C>A (p.Tyr208Ter) n.4045C>A c.408C>A (p.Tyr136Ter) c.277+1497C>A (n.277+1497C>A) c.*709C>A (n.*709C>A) c.1665C>A (p.Tyr555Ter) | |
| 16 | g.89935075C= | CA2242019889 | TUBB3 | c.624C= (p.Tyr208=) n.4045C= c.408C= (p.Tyr136=) c.277+1497C= (n.277+1497C=) c.*709C= (n.*709C=) c.1665C= (p.Tyr555=) | |
| 16 | g.89935075C>G | CA397474983 | TUBB3 | c.624C>G (p.Tyr208Ter) n.4045C>G c.408C>G (p.Tyr136Ter) c.277+1497C>G (n.277+1497C>G) c.*709C>G (n.*709C>G) c.1665C>G (p.Tyr555Ter) | gnomAD v4 |
| 16 | g.89935075C>T | CA497381455 | TUBB3 | c.624C>T (p.Tyr208=) n.4045C>T c.408C>T (p.Tyr136=) c.277+1497C>T (n.277+1497C>T) c.*709C>T (n.*709C>T) c.1665C>T (p.Tyr555=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935076G>A | CA397474984 | TUBB3 | c.625G>A (p.Asp209Asn) n.4046G>A c.409G>A (p.Asp137Asn) c.277+1498G>A (n.277+1498G>A) c.*710G>A (n.*710G>A) c.1666G>A (p.Asp556Asn) | dbSNP gnomAD v4 |
| 16 | g.89935076G>C | CA397474985 | TUBB3 | c.625G>C (p.Asp209His) n.4046G>C c.409G>C (p.Asp137His) c.277+1498G>C (n.277+1498G>C) c.*710G>C (n.*710G>C) c.1666G>C (p.Asp556His) | gnomAD v4 |
| 16 | g.89935076G= | CA2242019891 | TUBB3 | c.625G= (p.Asp209=) n.4046G= c.409G= (p.Asp137=) c.277+1498G= (n.277+1498G=) c.*710G= (n.*710G=) c.1666G= (p.Asp556=) | |
| 16 | g.89935076G>T | CA397474986 | TUBB3 | c.625G>T (p.Asp209Tyr) n.4046G>T c.409G>T (p.Asp137Tyr) c.277+1498G>T (n.277+1498G>T) c.*710G>T (n.*710G>T) c.1666G>T (p.Asp556Tyr) | |
| 16 | g.89935077A>C | CA397474987 | TUBB3 | c.626A>C (p.Asp209Ala) n.4047A>C c.410A>C (p.Asp137Ala) c.277+1499A>C (n.277+1499A>C) c.*711A>C (n.*711A>C) c.1667A>C (p.Asp556Ala) | |
| 16 | g.89935077A>G | CA397474988 | TUBB3 | c.626A>G (p.Asp209Gly) n.4047A>G c.410A>G (p.Asp137Gly) c.277+1499A>G (n.277+1499A>G) c.*711A>G (n.*711A>G) c.1667A>G (p.Asp556Gly) | |
| 16 | g.89935077A>T | CA397474989 | TUBB3 | c.626A>T (p.Asp209Val) n.4047A>T c.410A>T (p.Asp137Val) c.277+1499A>T (n.277+1499A>T) c.*711A>T (n.*711A>T) c.1667A>T (p.Asp556Val) | |
| 16 | g.89935078C>A | CA397474990 | TUBB3 | c.627C>A (p.Asp209Glu) n.4048C>A c.411C>A (p.Asp137Glu) c.277+1500C>A (n.277+1500C>A) c.*712C>A (n.*712C>A) c.1668C>A (p.Asp556Glu) | |
| 16 | g.89935078C>G | CA397474991 | TUBB3 | c.627C>G (p.Asp209Glu) n.4048C>G c.411C>G (p.Asp137Glu) c.277+1500C>G (n.277+1500C>G) c.*712C>G (n.*712C>G) c.1668C>G (p.Asp556Glu) | |
| 16 | g.89935078C>T | CA497381459 | TUBB3 | c.627C>T (p.Asp209=) n.4048C>T c.411C>T (p.Asp137=) c.277+1500C>T (n.277+1500C>T) c.*712C>T (n.*712C>T) c.1668C>T (p.Asp556=) | |
| 16 | g.89935079A>C | CA397474994 | TUBB3 | c.628A>C (p.Ile210Leu) n.4049A>C c.412A>C (p.Ile138Leu) c.277+1501A>C (n.277+1501A>C) c.*713A>C (n.*713A>C) c.1669A>C (p.Ile557Leu) | |
| 16 | g.89935079A>G | CA397474993 | TUBB3 | c.628A>G (p.Ile210Val) n.4049A>G c.412A>G (p.Ile138Val) c.277+1501A>G (n.277+1501A>G) c.*713A>G (n.*713A>G) c.1669A>G (p.Ile557Val) | gnomAD v4 |
| 16 | g.89935079A>T | CA397474992 | TUBB3 | c.628A>T (p.Ile210Phe) n.4049A>T c.412A>T (p.Ile138Phe) c.277+1501A>T (n.277+1501A>T) c.*713A>T (n.*713A>T) c.1669A>T (p.Ile557Phe) | |
| 16 | g.89935080T>A | CA397474995 | TUBB3 | c.629T>A (p.Ile210Asn) n.4050T>A c.413T>A (p.Ile138Asn) c.277+1502T>A (n.277+1502T>A) c.*714T>A (n.*714T>A) c.1670T>A (p.Ile557Asn) | |
| 16 | g.89935080T>C | CA397474996 | TUBB3 | c.629T>C (p.Ile210Thr) n.4050T>C c.413T>C (p.Ile138Thr) c.277+1502T>C (n.277+1502T>C) c.*714T>C (n.*714T>C) c.1670T>C (p.Ile557Thr) | |
| 16 | g.89935080T>G | CA397474997 | TUBB3 | c.629T>G (p.Ile210Ser) n.4050T>G c.413T>G (p.Ile138Ser) c.277+1502T>G (n.277+1502T>G) c.*714T>G (n.*714T>G) c.1670T>G (p.Ile557Ser) | |
| 16 | g.89935081C>A | CA497381467 | TUBB3 | c.630C>A (p.Ile210=) n.4051C>A c.414C>A (p.Ile138=) c.277+1503C>A (n.277+1503C>A) c.*715C>A (n.*715C>A) c.1671C>A (p.Ile557=) | gnomAD v4 |
| 16 | g.89935081C>G | CA397474998 | TUBB3 | c.630C>G (p.Ile210Met) n.4051C>G c.414C>G (p.Ile138Met) c.277+1503C>G (n.277+1503C>G) c.*715C>G (n.*715C>G) c.1671C>G (p.Ile557Met) | |
| 16 | g.89935081C>T | CA497381470 | TUBB3 | c.630C>T (p.Ile210=) n.4051C>T c.414C>T (p.Ile138=) c.277+1503C>T (n.277+1503C>T) c.*715C>T (n.*715C>T) c.1671C>T (p.Ile557=) | |
| 16 | g.89935083_89935085del | CA2635070802 | TUBB3 | c.632_634del (p.Cys211del) n.4053_4055del c.416_418del (p.Cys139del) c.277+1505_277+1507del (n.277+1505_277+1507del) c.*717_*719del (n.*717_*719del) c.1673_1675del (p.Cys558del) | gnomAD v4 |
| 16 | g.89935082T>A | CA397474999 | TUBB3 | c.631T>A (p.Cys211Ser) n.4052T>A c.415T>A (p.Cys139Ser) c.277+1504T>A (n.277+1504T>A) c.*716T>A (n.*716T>A) c.1672T>A (p.Cys558Ser) | |
| 16 | g.89935082T>C | CA397475000 | TUBB3 | c.631T>C (p.Cys211Arg) n.4052T>C c.415T>C (p.Cys139Arg) c.277+1504T>C (n.277+1504T>C) c.*716T>C (n.*716T>C) c.1672T>C (p.Cys558Arg) | ClinVar dbSNP |
| 16 | g.89935082T>G | CA397475001 | TUBB3 | c.631T>G (p.Cys211Gly) n.4052T>G c.415T>G (p.Cys139Gly) c.277+1504T>G (n.277+1504T>G) c.*716T>G (n.*716T>G) c.1672T>G (p.Cys558Gly) | |
| 16 | g.89935082T= | CA2242019895 | TUBB3 | c.631T= (p.Cys211=) n.4052T= c.415T= (p.Cys139=) c.277+1504T= (n.277+1504T=) c.*716T= (n.*716T=) c.1672T= (p.Cys558=) | |
| 16 | g.89935083G>A | CA397475002 | TUBB3 | c.632G>A (p.Cys211Tyr) n.4053G>A c.416G>A (p.Cys139Tyr) c.277+1505G>A (n.277+1505G>A) c.*717G>A (n.*717G>A) c.1673G>A (p.Cys558Tyr) | |
| 16 | g.89935083G>C | CA397475003 | TUBB3 | c.632G>C (p.Cys211Ser) n.4053G>C c.416G>C (p.Cys139Ser) c.277+1505G>C (n.277+1505G>C) c.*717G>C (n.*717G>C) c.1673G>C (p.Cys558Ser) | |
| 16 | g.89935083G>T | CA397475004 | TUBB3 | c.632G>T (p.Cys211Phe) n.4053G>T c.416G>T (p.Cys139Phe) c.277+1505G>T (n.277+1505G>T) c.*717G>T (n.*717G>T) c.1673G>T (p.Cys558Phe) | |
| 16 | g.89935084C>A | CA397475005 | TUBB3 | c.633C>A (p.Cys211Ter) n.4054C>A c.417C>A (p.Cys139Ter) c.277+1506C>A (n.277+1506C>A) c.*718C>A (n.*718C>A) c.1674C>A (p.Cys558Ter) | |
| 16 | g.89935084C= | CA2242019900 | TUBB3 | c.633C= (p.Cys211=) n.4054C= c.417C= (p.Cys139=) c.277+1506C= (n.277+1506C=) c.*718C= (n.*718C=) c.1674C= (p.Cys558=) | |
| 16 | g.89935084C>G | CA397475006 | TUBB3 | c.633C>G (p.Cys211Trp) n.4054C>G c.417C>G (p.Cys139Trp) c.277+1506C>G (n.277+1506C>G) c.*718C>G (n.*718C>G) c.1674C>G (p.Cys558Trp) | |
| 16 | g.89935084C>T | CA8256140 | TUBB3 | c.633C>T (p.Cys211=) n.4054C>T c.417C>T (p.Cys139=) c.277+1506C>T (n.277+1506C>T) c.*718C>T (n.*718C>T) c.1674C>T (p.Cys558=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935085T>A | CA397475009 | TUBB3 | c.634T>A (p.Phe212Ile) n.4055T>A c.418T>A (p.Phe140Ile) c.277+1507T>A (n.277+1507T>A) c.*719T>A (n.*719T>A) c.1675T>A (p.Phe559Ile) | |
| 16 | g.89935085T>C | CA397475008 | TUBB3 | c.634T>C (p.Phe212Leu) n.4055T>C c.418T>C (p.Phe140Leu) c.277+1507T>C (n.277+1507T>C) c.*719T>C (n.*719T>C) c.1675T>C (p.Phe559Leu) | |
| 16 | g.89935085T>G | CA397475007 | TUBB3 | c.634T>G (p.Phe212Val) n.4055T>G c.418T>G (p.Phe140Val) c.277+1507T>G (n.277+1507T>G) c.*719T>G (n.*719T>G) c.1675T>G (p.Phe559Val) | |
| 16 | g.89935086T>A | CA397475010 | TUBB3 | c.635T>A (p.Phe212Tyr) n.4056T>A c.419T>A (p.Phe140Tyr) c.277+1508T>A (n.277+1508T>A) c.*720T>A (n.*720T>A) c.1676T>A (p.Phe559Tyr) | |
| 16 | g.89935086T>C | CA397475012 | TUBB3 | c.635T>C (p.Phe212Ser) n.4056T>C c.419T>C (p.Phe140Ser) c.277+1508T>C (n.277+1508T>C) c.*720T>C (n.*720T>C) c.1676T>C (p.Phe559Ser) | |
| 16 | g.89935086T>G | CA397475011 | TUBB3 | c.635T>G (p.Phe212Cys) n.4056T>G c.419T>G (p.Phe140Cys) c.277+1508T>G (n.277+1508T>G) c.*720T>G (n.*720T>G) c.1676T>G (p.Phe559Cys) | |
| 16 | g.89935087C>A | CA397475013 | TUBB3 | c.636C>A (p.Phe212Leu) n.4057C>A c.420C>A (p.Phe140Leu) c.277+1509C>A (n.277+1509C>A) c.*721C>A (n.*721C>A) c.1677C>A (p.Phe559Leu) | |
| 16 | g.89935087C= | CA2242019903 | TUBB3 | c.636C= (p.Phe212=) n.4057C= c.420C= (p.Phe140=) c.277+1509C= (n.277+1509C=) c.*721C= (n.*721C=) c.1677C= (p.Phe559=) | |
| 16 | g.89935087C>G | CA397475014 | TUBB3 | c.636C>G (p.Phe212Leu) n.4057C>G c.420C>G (p.Phe140Leu) c.277+1509C>G (n.277+1509C>G) c.*721C>G (n.*721C>G) c.1677C>G (p.Phe559Leu) | |
| 16 | g.89935087C>T | CA8256141 | TUBB3 | c.636C>T (p.Phe212=) n.4057C>T c.420C>T (p.Phe140=) c.277+1509C>T (n.277+1509C>T) c.*721C>T (n.*721C>T) c.1677C>T (p.Phe559=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935088C>A | CA397475015 | TUBB3 | c.637C>A (p.Arg213Ser) n.4058C>A c.421C>A (p.Arg141Ser) c.277+1510C>A (n.277+1510C>A) c.*722C>A (n.*722C>A) c.1678C>A (p.Arg560Ser) | COSMIC |
| 16 | g.89935088C>G | CA397475016 | TUBB3 | c.637C>G (p.Arg213Gly) n.4058C>G c.421C>G (p.Arg141Gly) c.277+1510C>G (n.277+1510C>G) c.*722C>G (n.*722C>G) c.1678C>G (p.Arg560Gly) | |
| 16 | g.89935088C>T | CA397475017 | TUBB3 | c.637C>T (p.Arg213Cys) n.4058C>T c.421C>T (p.Arg141Cys) c.277+1510C>T (n.277+1510C>T) c.*722C>T (n.*722C>T) c.1678C>T (p.Arg560Cys) | gnomAD v4 COSMIC |
| 16 | g.89935089G>A | CA8256142 | TUBB3 | c.638G>A (p.Arg213His) n.4059G>A c.422G>A (p.Arg141His) c.277+1511G>A (n.277+1511G>A) c.*723G>A (n.*723G>A) c.1679G>A (p.Arg560His) | ClinVar dbSNP ExAC gnomAD v4 |
| 16 | g.89935089G>C | CA397475018 | TUBB3 | c.638G>C (p.Arg213Pro) n.4059G>C c.422G>C (p.Arg141Pro) c.277+1511G>C (n.277+1511G>C) c.*723G>C (n.*723G>C) c.1679G>C (p.Arg560Pro) | |
| 16 | g.89935089G= | CA2242019905 | TUBB3 | c.638G= (p.Arg213=) n.4059G= c.422G= (p.Arg141=) c.277+1511G= (n.277+1511G=) c.*723G= (n.*723G=) c.1679G= (p.Arg560=) | |
| 16 | g.89935089G>T | CA397475019 | TUBB3 | c.638G>T (p.Arg213Leu) n.4059G>T c.422G>T (p.Arg141Leu) c.277+1511G>T (n.277+1511G>T) c.*723G>T (n.*723G>T) c.1679G>T (p.Arg560Leu) | |
| 16 | g.89935090C>A | CA497381494 | TUBB3 | c.639C>A (p.Arg213=) n.4060C>A c.423C>A (p.Arg141=) c.277+1512C>A (n.277+1512C>A) c.*724C>A (n.*724C>A) c.1680C>A (p.Arg560=) | |
| 16 | g.89935090C= | CA2242019908 | TUBB3 | c.639C= (p.Arg213=) n.4060C= c.423C= (p.Arg141=) c.277+1512C= (n.277+1512C=) c.*724C= (n.*724C=) c.1680C= (p.Arg560=) | |
| 16 | g.89935090C>G | CA497381491 | TUBB3 | c.639C>G (p.Arg213=) n.4060C>G c.423C>G (p.Arg141=) c.277+1512C>G (n.277+1512C>G) c.*724C>G (n.*724C>G) c.1680C>G (p.Arg560=) | |
| 16 | g.89935090C>T | CA8256143 | TUBB3 | c.639C>T (p.Arg213=) n.4060C>T c.423C>T (p.Arg141=) c.277+1512C>T (n.277+1512C>T) c.*724C>T (n.*724C>T) c.1680C>T (p.Arg560=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935091A= | CA2242019912 | TUBB3 | c.640A= (p.Thr214=) n.4061A= c.424A= (p.Thr142=) c.277+1513A= (n.277+1513A=) c.*725A= (n.*725A=) c.1681A= (p.Thr561=) | |
| 16 | g.89935091A>C | CA397475020 | TUBB3 | c.640A>C (p.Thr214Pro) n.4061A>C c.424A>C (p.Thr142Pro) c.277+1513A>C (n.277+1513A>C) c.*725A>C (n.*725A>C) c.1681A>C (p.Thr561Pro) | dbSNP |
| 16 | g.89935091A>G | CA397475021 | TUBB3 | c.640A>G (p.Thr214Ala) n.4061A>G c.424A>G (p.Thr142Ala) c.277+1513A>G (n.277+1513A>G) c.*725A>G (n.*725A>G) c.1681A>G (p.Thr561Ala) | |
| 16 | g.89935091A>T | CA397475022 | TUBB3 | c.640A>T (p.Thr214Ser) n.4061A>T c.424A>T (p.Thr142Ser) c.277+1513A>T (n.277+1513A>T) c.*725A>T (n.*725A>T) c.1681A>T (p.Thr561Ser) | |
| 16 | g.89935092C>A | CA397475025 | TUBB3 | c.641C>A (p.Thr214Asn) n.4062C>A c.425C>A (p.Thr142Asn) c.277+1514C>A (n.277+1514C>A) c.*726C>A (n.*726C>A) c.1682C>A (p.Thr561Asn) | |
| 16 | g.89935092C>G | CA397475023 | TUBB3 | c.641C>G (p.Thr214Ser) n.4062C>G c.425C>G (p.Thr142Ser) c.277+1514C>G (n.277+1514C>G) c.*726C>G (n.*726C>G) c.1682C>G (p.Thr561Ser) | |
| 16 | g.89935092C>T | CA397475024 | TUBB3 | c.641C>T (p.Thr214Ile) n.4062C>T c.425C>T (p.Thr142Ile) c.277+1514C>T (n.277+1514C>T) c.*726C>T (n.*726C>T) c.1682C>T (p.Thr561Ile) | |
| 16 | g.89935093C>A | CA497381500 | TUBB3 | c.642C>A (p.Thr214=) n.4063C>A c.426C>A (p.Thr142=) c.277+1515C>A (n.277+1515C>A) c.*727C>A (n.*727C>A) c.1683C>A (p.Thr561=) | gnomAD v4 |
| 16 | g.89935093C>G | CA497381502 | TUBB3 | c.642C>G (p.Thr214=) n.4063C>G c.426C>G (p.Thr142=) c.277+1515C>G (n.277+1515C>G) c.*727C>G (n.*727C>G) c.1683C>G (p.Thr561=) | |
| 16 | g.89935093C>T | CA497381501 | TUBB3 | c.642C>T (p.Thr214=) n.4063C>T c.426C>T (p.Thr142=) c.277+1515C>T (n.277+1515C>T) c.*727C>T (n.*727C>T) c.1683C>T (p.Thr561=) | |
| 16 | g.89935094C>A | CA397475026 | TUBB3 | c.643C>A (p.Leu215Ile) n.4064C>A c.427C>A (p.Leu143Ile) c.277+1516C>A (n.277+1516C>A) c.*728C>A (n.*728C>A) c.1684C>A (p.Leu562Ile) | |
| 16 | g.89935094C>G | CA397475027 | TUBB3 | c.643C>G (p.Leu215Val) n.4064C>G c.427C>G (p.Leu143Val) c.277+1516C>G (n.277+1516C>G) c.*728C>G (n.*728C>G) c.1684C>G (p.Leu562Val) | |
| 16 | g.89935094C>T | CA397475028 | TUBB3 | c.643C>T (p.Leu215Phe) n.4064C>T c.427C>T (p.Leu143Phe) c.277+1516C>T (n.277+1516C>T) c.*728C>T (n.*728C>T) c.1684C>T (p.Leu562Phe) | COSMIC |
| 16 | g.89935095T>A | CA397475029 | TUBB3 | c.644T>A (p.Leu215His) n.4065T>A c.428T>A (p.Leu143His) c.277+1517T>A (n.277+1517T>A) c.*729T>A (n.*729T>A) c.1685T>A (p.Leu562His) | ClinVar dbSNP |
| 16 | g.89935095T>C | CA397475030 | TUBB3 | c.644T>C (p.Leu215Pro) n.4065T>C c.428T>C (p.Leu143Pro) c.277+1517T>C (n.277+1517T>C) c.*729T>C (n.*729T>C) c.1685T>C (p.Leu562Pro) | |
| 16 | g.89935095T>G | CA397475031 | TUBB3 | c.644T>G (p.Leu215Arg) n.4065T>G c.428T>G (p.Leu143Arg) c.277+1517T>G (n.277+1517T>G) c.*729T>G (n.*729T>G) c.1685T>G (p.Leu562Arg) | |
| 16 | g.89935096C>A | CA497381510 | TUBB3 | c.645C>A (p.Leu215=) n.4066C>A c.429C>A (p.Leu143=) c.277+1518C>A (n.277+1518C>A) c.*730C>A (n.*730C>A) c.1686C>A (p.Leu562=) | |
| 16 | g.89935096C= | CA2242019915 | TUBB3 | c.645C= (p.Leu215=) n.4066C= c.429C= (p.Leu143=) c.277+1518C= (n.277+1518C=) c.*730C= (n.*730C=) c.1686C= (p.Leu562=) | |
| 16 | g.89935096C>G | CA497381512 | TUBB3 | c.645C>G (p.Leu215=) n.4066C>G c.429C>G (p.Leu143=) c.277+1518C>G (n.277+1518C>G) c.*730C>G (n.*730C>G) c.1686C>G (p.Leu562=) | |
| 16 | g.89935096C>T | CA497381514 | TUBB3 | c.645C>T (p.Leu215=) n.4066C>T c.429C>T (p.Leu143=) c.277+1518C>T (n.277+1518C>T) c.*730C>T (n.*730C>T) c.1686C>T (p.Leu562=) | dbSNP |
| 16 | g.89935097A>C | CA397475032 | TUBB3 | c.646A>C (p.Lys216Gln) n.4067A>C c.430A>C (p.Lys144Gln) c.277+1519A>C (n.277+1519A>C) c.*731A>C (n.*731A>C) c.1687A>C (p.Lys563Gln) | |
| 16 | g.89935097A>G | CA397475033 | TUBB3 | c.646A>G (p.Lys216Glu) n.4067A>G c.430A>G (p.Lys144Glu) c.277+1519A>G (n.277+1519A>G) c.*731A>G (n.*731A>G) c.1687A>G (p.Lys563Glu) | |
| 16 | g.89935097A>T | CA397475034 | TUBB3 | c.646A>T (p.Lys216Ter) n.4067A>T c.430A>T (p.Lys144Ter) c.277+1519A>T (n.277+1519A>T) c.*731A>T (n.*731A>T) c.1687A>T (p.Lys563Ter) | |
| 16 | g.89935098A>C | CA397475035 | TUBB3 | c.647A>C (p.Lys216Thr) n.4068A>C c.431A>C (p.Lys144Thr) c.277+1520A>C (n.277+1520A>C) c.*732A>C (n.*732A>C) c.1688A>C (p.Lys563Thr) | |
| 16 | g.89935098A>G | CA397475036 | TUBB3 | c.647A>G (p.Lys216Arg) n.4068A>G c.431A>G (p.Lys144Arg) c.277+1520A>G (n.277+1520A>G) c.*732A>G (n.*732A>G) c.1688A>G (p.Lys563Arg) | ClinVar |
| 16 | g.89935098A>T | CA397475037 | TUBB3 | c.647A>T (p.Lys216Met) n.4068A>T c.431A>T (p.Lys144Met) c.277+1520A>T (n.277+1520A>T) c.*732A>T (n.*732A>T) c.1688A>T (p.Lys563Met) | |
| 16 | g.89935099G>A | CA497381518 | TUBB3 | c.648G>A (p.Lys216=) n.4069G>A c.432G>A (p.Lys144=) c.277+1521G>A (n.277+1521G>A) c.*733G>A (n.*733G>A) c.1689G>A (p.Lys563=) | |
| 16 | g.89935099G>C | CA397475038 | TUBB3 | c.648G>C (p.Lys216Asn) n.4069G>C c.432G>C (p.Lys144Asn) c.277+1521G>C (n.277+1521G>C) c.*733G>C (n.*733G>C) c.1689G>C (p.Lys563Asn) | |
| 16 | g.89935099G>T | CA397475039 | TUBB3 | c.648G>T (p.Lys216Asn) n.4069G>T c.432G>T (p.Lys144Asn) c.277+1521G>T (n.277+1521G>T) c.*733G>T (n.*733G>T) c.1689G>T (p.Lys563Asn) | |
| 16 | g.89935100C>A | CA397475040 | TUBB3 | c.649C>A (p.Leu217Met) n.4070C>A c.433C>A (p.Leu145Met) c.277+1522C>A (n.277+1522C>A) c.*734C>A (n.*734C>A) c.1690C>A (p.Leu564Met) | |
| 16 | g.89935100C>G | CA397475041 | TUBB3 | c.649C>G (p.Leu217Val) n.4070C>G c.433C>G (p.Leu145Val) c.277+1522C>G (n.277+1522C>G) c.*734C>G (n.*734C>G) c.1690C>G (p.Leu564Val) | |
| 16 | g.89935100C>T | CA497381010 | TUBB3 | c.649C>T (p.Leu217=) n.4070C>T c.433C>T (p.Leu145=) c.277+1522C>T (n.277+1522C>T) c.*734C>T (n.*734C>T) c.1690C>T (p.Leu564=) | gnomAD v4 |
| 16 | g.89935101T>A | CA397475042 | TUBB3 | c.650T>A (p.Leu217Gln) n.4071T>A c.434T>A (p.Leu145Gln) c.277+1523T>A (n.277+1523T>A) c.*735T>A (n.*735T>A) c.1691T>A (p.Leu564Gln) | |
| 16 | g.89935101T>C | CA397475043 | TUBB3 | c.650T>C (p.Leu217Pro) n.4071T>C c.434T>C (p.Leu145Pro) c.277+1523T>C (n.277+1523T>C) c.*735T>C (n.*735T>C) c.1691T>C (p.Leu564Pro) | |
| 16 | g.89935101T>G | CA397475044 | TUBB3 | c.650T>G (p.Leu217Arg) n.4071T>G c.434T>G (p.Leu145Arg) c.277+1523T>G (n.277+1523T>G) c.*735T>G (n.*735T>G) c.1691T>G (p.Leu564Arg) | |
| 16 | g.89935102G>A | CA8256144 | TUBB3 | c.651G>A (p.Leu217=) n.4072G>A c.435G>A (p.Leu145=) c.277+1524G>A (n.277+1524G>A) c.*736G>A (n.*736G>A) c.1692G>A (p.Leu564=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935102G>C | CA497381015 | TUBB3 | c.651G>C (p.Leu217=) n.4072G>C c.435G>C (p.Leu145=) c.277+1524G>C (n.277+1524G>C) c.*736G>C (n.*736G>C) c.1692G>C (p.Leu564=) | |
| 16 | g.89935102G= | CA2242019919 | TUBB3 | c.651G= (p.Leu217=) n.4072G= c.435G= (p.Leu145=) c.277+1524G= (n.277+1524G=) c.*736G= (n.*736G=) c.1692G= (p.Leu564=) | |
| 16 | g.89935102G>T | CA497381016 | TUBB3 | c.651G>T (p.Leu217=) n.4072G>T c.435G>T (p.Leu145=) c.277+1524G>T (n.277+1524G>T) c.*736G>T (n.*736G>T) c.1692G>T (p.Leu564=) | |
| 16 | g.89935103G>A | CA397475045 | TUBB3 | c.652G>A (p.Ala218Thr) n.4073G>A c.436G>A (p.Ala146Thr) c.277+1525G>A (n.277+1525G>A) c.*737G>A (n.*737G>A) c.1693G>A (p.Ala565Thr) | gnomAD v4 COSMIC |
| 16 | g.89935103G>C | CA397475046 | TUBB3 | c.652G>C (p.Ala218Pro) n.4073G>C c.436G>C (p.Ala146Pro) c.277+1525G>C (n.277+1525G>C) c.*737G>C (n.*737G>C) c.1693G>C (p.Ala565Pro) | |
| 16 | g.89935103G>T | CA397475047 | TUBB3 | c.652G>T (p.Ala218Ser) n.4073G>T c.436G>T (p.Ala146Ser) c.277+1525G>T (n.277+1525G>T) c.*737G>T (n.*737G>T) c.1693G>T (p.Ala565Ser) | |
| 16 | g.89935104C>A | CA397475048 | TUBB3 | c.653C>A (p.Ala218Asp) n.4074C>A c.437C>A (p.Ala146Asp) c.277+1526C>A (n.277+1526C>A) c.*738C>A (n.*738C>A) c.1694C>A (p.Ala565Asp) | |
| 16 | g.89935104C>G | CA397475049 | TUBB3 | c.653C>G (p.Ala218Gly) n.4074C>G c.437C>G (p.Ala146Gly) c.277+1526C>G (n.277+1526C>G) c.*738C>G (n.*738C>G) c.1694C>G (p.Ala565Gly) | |
| 16 | g.89935104C>T | CA397475050 | TUBB3 | c.653C>T (p.Ala218Val) n.4074C>T c.437C>T (p.Ala146Val) c.277+1526C>T (n.277+1526C>T) c.*738C>T (n.*738C>T) c.1694C>T (p.Ala565Val) | |
| 16 | g.89935105C>A | CA497381018 | TUBB3 | c.654C>A (p.Ala218=) n.4075C>A c.438C>A (p.Ala146=) c.277+1527C>A (n.277+1527C>A) c.*739C>A (n.*739C>A) c.1695C>A (p.Ala565=) | |
| 16 | g.89935105C>G | CA497381019 | TUBB3 | c.654C>G (p.Ala218=) n.4075C>G c.438C>G (p.Ala146=) c.277+1527C>G (n.277+1527C>G) c.*739C>G (n.*739C>G) c.1695C>G (p.Ala565=) | |
| 16 | g.89935105C>T | CA497381020 | TUBB3 | c.654C>T (p.Ala218=) n.4075C>T c.438C>T (p.Ala146=) c.277+1527C>T (n.277+1527C>T) c.*739C>T (n.*739C>T) c.1695C>T (p.Ala565=) | |
| 16 | g.89935106A>C | CA397475052 | TUBB3 | c.655A>C (p.Thr219Pro) n.4076A>C c.439A>C (p.Thr147Pro) c.277+1528A>C (n.277+1528A>C) c.*740A>C (n.*740A>C) c.1696A>C (p.Thr566Pro) | |
| 16 | g.89935106A>G | CA397475053 | TUBB3 | c.655A>G (p.Thr219Ala) n.4076A>G c.439A>G (p.Thr147Ala) c.277+1528A>G (n.277+1528A>G) c.*740A>G (n.*740A>G) c.1696A>G (p.Thr566Ala) | |
| 16 | g.89935106A>T | CA397475051 | TUBB3 | c.655A>T (p.Thr219Ser) n.4076A>T c.439A>T (p.Thr147Ser) c.277+1528A>T (n.277+1528A>T) c.*740A>T (n.*740A>T) c.1696A>T (p.Thr566Ser) | |
| 16 | g.89935107C>A | CA397475054 | TUBB3 | c.656C>A (p.Thr219Lys) n.4077C>A c.440C>A (p.Thr147Lys) c.277+1529C>A (n.277+1529C>A) c.*741C>A (n.*741C>A) c.1697C>A (p.Thr566Lys) | |
| 16 | g.89935107C>G | CA397475055 | TUBB3 | c.656C>G (p.Thr219Arg) n.4077C>G c.440C>G (p.Thr147Arg) c.277+1529C>G (n.277+1529C>G) c.*741C>G (n.*741C>G) c.1697C>G (p.Thr566Arg) | |
| 16 | g.89935107C>T | CA397475056 | TUBB3 | c.656C>T (p.Thr219Met) n.4077C>T c.440C>T (p.Thr147Met) c.277+1529C>T (n.277+1529C>T) c.*741C>T (n.*741C>T) c.1697C>T (p.Thr566Met) | gnomAD v4 |
| 16 | g.89935108G>A | CA8256145 | TUBB3 | c.657G>A (p.Thr219=) n.4078G>A c.441G>A (p.Thr147=) c.277+1530G>A (n.277+1530G>A) c.*742G>A (n.*742G>A) c.1698G>A (p.Thr566=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935108G>C | CA497381025 | TUBB3 | c.657G>C (p.Thr219=) n.4078G>C c.441G>C (p.Thr147=) c.277+1530G>C (n.277+1530G>C) c.*742G>C (n.*742G>C) c.1698G>C (p.Thr566=) | |
| 16 | g.89935108G= | CA2242019925 | TUBB3 | c.657G= (p.Thr219=) n.4078G= c.441G= (p.Thr147=) c.277+1530G= (n.277+1530G=) c.*742G= (n.*742G=) c.1698G= (p.Thr566=) | |
| 16 | g.89935108G>T | CA497381023 | TUBB3 | c.657G>T (p.Thr219=) n.4078G>T c.441G>T (p.Thr147=) c.277+1530G>T (n.277+1530G>T) c.*742G>T (n.*742G>T) c.1698G>T (p.Thr566=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935109C>A | CA397475059 | TUBB3 | c.658C>A (p.Pro220Thr) n.4079C>A c.442C>A (p.Pro148Thr) c.277+1531C>A (n.277+1531C>A) c.*743C>A (n.*743C>A) c.1699C>A (p.Pro567Thr) | |
| 16 | g.89935109C>G | CA397475058 | TUBB3 | c.658C>G (p.Pro220Ala) n.4079C>G c.442C>G (p.Pro148Ala) c.277+1531C>G (n.277+1531C>G) c.*743C>G (n.*743C>G) c.1699C>G (p.Pro567Ala) | |
| 16 | g.89935109C>T | CA397475057 | TUBB3 | c.658C>T (p.Pro220Ser) n.4079C>T c.442C>T (p.Pro148Ser) c.277+1531C>T (n.277+1531C>T) c.*743C>T (n.*743C>T) c.1699C>T (p.Pro567Ser) | |
| 16 | g.89935110C>A | CA397475060 | TUBB3 | c.659C>A (p.Pro220His) n.4080C>A c.443C>A (p.Pro148His) c.277+1532C>A (n.277+1532C>A) c.*744C>A (n.*744C>A) c.1700C>A (p.Pro567His) | |
| 16 | g.89935110C>G | CA397475061 | TUBB3 | c.659C>G (p.Pro220Arg) n.4080C>G c.443C>G (p.Pro148Arg) c.277+1532C>G (n.277+1532C>G) c.*744C>G (n.*744C>G) c.1700C>G (p.Pro567Arg) | |
| 16 | g.89935110C>T | CA397475062 | TUBB3 | c.659C>T (p.Pro220Leu) n.4080C>T c.443C>T (p.Pro148Leu) c.277+1532C>T (n.277+1532C>T) c.*744C>T (n.*744C>T) c.1700C>T (p.Pro567Leu) | |
| 16 | g.89935111C>A | CA497381031 | TUBB3 | c.660C>A (p.Pro220=) n.4081C>A c.444C>A (p.Pro148=) c.277+1533C>A (n.277+1533C>A) c.*745C>A (n.*745C>A) c.1701C>A (p.Pro567=) | |
| 16 | g.89935111C= | CA2242019930 | TUBB3 | c.660C= (p.Pro220=) n.4081C= c.444C= (p.Pro148=) c.277+1533C= (n.277+1533C=) c.*745C= (n.*745C=) c.1701C= (p.Pro567=) | |
| 16 | g.89935111C>G | CA497381033 | TUBB3 | c.660C>G (p.Pro220=) n.4081C>G c.444C>G (p.Pro148=) c.277+1533C>G (n.277+1533C>G) c.*745C>G (n.*745C>G) c.1701C>G (p.Pro567=) | |
| 16 | g.89935111C>T | CA497381032 | TUBB3 | c.660C>T (p.Pro220=) n.4081C>T c.444C>T (p.Pro148=) c.277+1533C>T (n.277+1533C>T) c.*745C>T (n.*745C>T) c.1701C>T (p.Pro567=) | dbSNP gnomAD v4 |
| 16 | g.89935112A>C | CA397475063 | TUBB3 | c.661A>C (p.Thr221Pro) n.4082A>C c.445A>C (p.Thr149Pro) c.277+1534A>C (n.277+1534A>C) c.*746A>C (n.*746A>C) c.1702A>C (p.Thr568Pro) | |
| 16 | g.89935112A>G | CA397475064 | TUBB3 | c.661A>G (p.Thr221Ala) n.4082A>G c.445A>G (p.Thr149Ala) c.277+1534A>G (n.277+1534A>G) c.*746A>G (n.*746A>G) c.1702A>G (p.Thr568Ala) | |
| 16 | g.89935112A>T | CA397475065 | TUBB3 | c.661A>T (p.Thr221Ser) n.4082A>T c.445A>T (p.Thr149Ser) c.277+1534A>T (n.277+1534A>T) c.*746A>T (n.*746A>T) c.1702A>T (p.Thr568Ser) | |
| 16 | g.89935113C>A | CA8256146 | TUBB3 | c.662C>A (p.Thr221Asn) n.4083C>A c.446C>A (p.Thr149Asn) c.277+1535C>A (n.277+1535C>A) c.*747C>A (n.*747C>A) c.1703C>A (p.Thr568Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935113C= | CA2242019932 | TUBB3 | c.662C= (p.Thr221=) n.4083C= c.446C= (p.Thr149=) c.277+1535C= (n.277+1535C=) c.*747C= (n.*747C=) c.1703C= (p.Thr568=) | |
| 16 | g.89935113C>G | CA397475067 | TUBB3 | c.662C>G (p.Thr221Ser) n.4083C>G c.446C>G (p.Thr149Ser) c.277+1535C>G (n.277+1535C>G) c.*747C>G (n.*747C>G) c.1703C>G (p.Thr568Ser) | |
| 16 | g.89935113C>T | CA397475066 | TUBB3 | c.662C>T (p.Thr221Ile) n.4083C>T c.446C>T (p.Thr149Ile) c.277+1535C>T (n.277+1535C>T) c.*747C>T (n.*747C>T) c.1703C>T (p.Thr568Ile) | gnomAD v4 |
| 16 | g.89935114del | CA2576104231 | TUBB3 | c.663del (p.Tyr222ThrfsTer12) n.4084del c.447del (p.Tyr150ThrfsTer12) c.277+1536del (n.277+1536del) c.*748del (n.*748del) c.1704del (p.Tyr569ThrfsTer12) | |
| 16 | g.89935114C>A | CA497381040 | TUBB3 | c.663C>A (p.Thr221=) n.4084C>A c.447C>A (p.Thr149=) c.277+1536C>A (n.277+1536C>A) c.*748C>A (n.*748C>A) c.1704C>A (p.Thr568=) | gnomAD v4 |
| 16 | g.89935114C= | CA2242019934 | TUBB3 | c.663C= (p.Thr221=) n.4084C= c.447C= (p.Thr149=) c.277+1536C= (n.277+1536C=) c.*748C= (n.*748C=) c.1704C= (p.Thr568=) | |
| 16 | g.89935114C>G | CA497381042 | TUBB3 | c.663C>G (p.Thr221=) n.4084C>G c.447C>G (p.Thr149=) c.277+1536C>G (n.277+1536C>G) c.*748C>G (n.*748C>G) c.1704C>G (p.Thr568=) | |
| 16 | g.89935114C>T | CA8256147 | TUBB3 | c.663C>T (p.Thr221=) n.4084C>T c.447C>T (p.Thr149=) c.277+1536C>T (n.277+1536C>T) c.*748C>T (n.*748C>T) c.1704C>T (p.Thr568=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935115T>A | CA397475069 | TUBB3 | c.664T>A (p.Tyr222Asn) n.4085T>A c.448T>A (p.Tyr150Asn) c.277+1537T>A (n.277+1537T>A) c.*749T>A (n.*749T>A) c.1705T>A (p.Tyr569Asn) | |
| 16 | g.89935115T>C | CA397475068 | TUBB3 | c.664T>C (p.Tyr222His) n.4085T>C c.448T>C (p.Tyr150His) c.277+1537T>C (n.277+1537T>C) c.*749T>C (n.*749T>C) c.1705T>C (p.Tyr569His) | |
| 16 | g.89935115T>G | CA397475070 | TUBB3 | c.664T>G (p.Tyr222Asp) n.4085T>G c.448T>G (p.Tyr150Asp) c.277+1537T>G (n.277+1537T>G) c.*749T>G (n.*749T>G) c.1705T>G (p.Tyr569Asp) | |
| 16 | g.89935116A>C | CA397475071 | TUBB3 | c.665A>C (p.Tyr222Ser) n.4086A>C c.449A>C (p.Tyr150Ser) c.277+1538A>C (n.277+1538A>C) c.*750A>C (n.*750A>C) c.1706A>C (p.Tyr569Ser) | |
| 16 | g.89935116A>G | CA397475072 | TUBB3 | c.665A>G (p.Tyr222Cys) n.4086A>G c.449A>G (p.Tyr150Cys) c.277+1538A>G (n.277+1538A>G) c.*750A>G (n.*750A>G) c.1706A>G (p.Tyr569Cys) | gnomAD v4 |
| 16 | g.89935116A>T | CA397475073 | TUBB3 | c.665A>T (p.Tyr222Phe) n.4086A>T c.449A>T (p.Tyr150Phe) c.277+1538A>T (n.277+1538A>T) c.*750A>T (n.*750A>T) c.1706A>T (p.Tyr569Phe) | |
| 16 | g.89935117C>A | CA397475074 | TUBB3 | c.666C>A (p.Tyr222Ter) n.4087C>A c.450C>A (p.Tyr150Ter) c.277+1539C>A (n.277+1539C>A) c.*751C>A (n.*751C>A) c.1707C>A (p.Tyr569Ter) | |
| 16 | g.89935117C= | CA2242019940 | TUBB3 | c.666C= (p.Tyr222=) n.4087C= c.450C= (p.Tyr150=) c.277+1539C= (n.277+1539C=) c.*751C= (n.*751C=) c.1707C= (p.Tyr569=) | |
| 16 | g.89935117C>G | CA397475075 | TUBB3 | c.666C>G (p.Tyr222Ter) n.4087C>G c.450C>G (p.Tyr150Ter) c.277+1539C>G (n.277+1539C>G) c.*751C>G (n.*751C>G) c.1707C>G (p.Tyr569Ter) | |
| 16 | g.89935117C>T | CA173796 | TUBB3 | c.666C>T (p.Tyr222=) n.4087C>T c.450C>T (p.Tyr150=) c.277+1539C>T (n.277+1539C>T) c.*751C>T (n.*751C>T) c.1707C>T (p.Tyr569=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89935118G>A | CA8256148 | TUBB3 | c.667G>A (p.Gly223Arg) n.4088G>A c.451G>A (p.Gly151Arg) c.277+1540G>A (n.277+1540G>A) c.*752G>A (n.*752G>A) c.1708G>A (p.Gly570Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935118G>C | CA397475076 | TUBB3 | c.667G>C (p.Gly223Arg) n.4088G>C c.451G>C (p.Gly151Arg) c.277+1540G>C (n.277+1540G>C) c.*752G>C (n.*752G>C) c.1708G>C (p.Gly570Arg) | |
| 16 | g.89935118G= | CA2242019942 | TUBB3 | c.667G= (p.Gly223=) n.4088G= c.451G= (p.Gly151=) c.277+1540G= (n.277+1540G=) c.*752G= (n.*752G=) c.1708G= (p.Gly570=) | |
| 16 | g.89935118G>T | CA397475077 | TUBB3 | c.667G>T (p.Gly223Trp) n.4088G>T c.451G>T (p.Gly151Trp) c.277+1540G>T (n.277+1540G>T) c.*752G>T (n.*752G>T) c.1708G>T (p.Gly570Trp) | |
| 16 | g.89935119G>A | CA397475078 | TUBB3 | c.668G>A (p.Gly223Glu) n.4089G>A c.452G>A (p.Gly151Glu) c.277+1541G>A (n.277+1541G>A) c.*753G>A (n.*753G>A) c.1709G>A (p.Gly570Glu) | gnomAD v4 |
| 16 | g.89935119G>C | CA397475079 | TUBB3 | c.668G>C (p.Gly223Ala) n.4089G>C c.452G>C (p.Gly151Ala) c.277+1541G>C (n.277+1541G>C) c.*753G>C (n.*753G>C) c.1709G>C (p.Gly570Ala) | dbSNP |
| 16 | g.89935119G>T | CA397475080 | TUBB3 | c.668G>T (p.Gly223Val) n.4089G>T c.452G>T (p.Gly151Val) c.277+1541G>T (n.277+1541G>T) c.*753G>T (n.*753G>T) c.1709G>T (p.Gly570Val) | |
| 16 | g.89935120G>A | CA497381049 | TUBB3 | c.669G>A (p.Gly223=) n.4090G>A c.453G>A (p.Gly151=) c.277+1542G>A (n.277+1542G>A) c.*754G>A (n.*754G>A) c.1710G>A (p.Gly570=) | |
| 16 | g.89935120G>C | CA497381048 | TUBB3 | c.669G>C (p.Gly223=) n.4090G>C c.453G>C (p.Gly151=) c.277+1542G>C (n.277+1542G>C) c.*754G>C (n.*754G>C) c.1710G>C (p.Gly570=) | |
| 16 | g.89935120G>T | CA497381047 | TUBB3 | c.669G>T (p.Gly223=) n.4090G>T c.453G>T (p.Gly151=) c.277+1542G>T (n.277+1542G>T) c.*754G>T (n.*754G>T) c.1710G>T (p.Gly570=) | dbSNP |
| 16 | g.89935121G>A | CA397475083 | TUBB3 | c.670G>A (p.Asp224Asn) n.4091G>A c.454G>A (p.Asp152Asn) c.277+1543G>A (n.277+1543G>A) c.*755G>A (n.*755G>A) c.1711G>A (p.Asp571Asn) | ClinVar |
| 16 | g.89935121G>C | CA397475082 | TUBB3 | c.670G>C (p.Asp224His) n.4091G>C c.454G>C (p.Asp152His) c.277+1543G>C (n.277+1543G>C) c.*755G>C (n.*755G>C) c.1711G>C (p.Asp571His) | |
| 16 | g.89935121G>T | CA397475081 | TUBB3 | c.670G>T (p.Asp224Tyr) n.4091G>T c.454G>T (p.Asp152Tyr) c.277+1543G>T (n.277+1543G>T) c.*755G>T (n.*755G>T) c.1711G>T (p.Asp571Tyr) | |
| 16 | g.89935122A>C | CA397475084 | TUBB3 | c.671A>C (p.Asp224Ala) n.4092A>C c.455A>C (p.Asp152Ala) c.277+1544A>C (n.277+1544A>C) c.*756A>C (n.*756A>C) c.1712A>C (p.Asp571Ala) | |
| 16 | g.89935122A>G | CA397475085 | TUBB3 | c.671A>G (p.Asp224Gly) n.4092A>G c.455A>G (p.Asp152Gly) c.277+1544A>G (n.277+1544A>G) c.*756A>G (n.*756A>G) c.1712A>G (p.Asp571Gly) | |
| 16 | g.89935122A>T | CA397475086 | TUBB3 | c.671A>T (p.Asp224Val) n.4092A>T c.455A>T (p.Asp152Val) c.277+1544A>T (n.277+1544A>T) c.*756A>T (n.*756A>T) c.1712A>T (p.Asp571Val) | |
| 16 | g.89935123C>A | CA397475087 | TUBB3 | c.672C>A (p.Asp224Glu) n.4093C>A c.456C>A (p.Asp152Glu) c.277+1545C>A (n.277+1545C>A) c.*757C>A (n.*757C>A) c.1713C>A (p.Asp571Glu) | |
| 16 | g.89935123C= | CA2242019945 | TUBB3 | c.672C= (p.Asp224=) n.4093C= c.456C= (p.Asp152=) c.277+1545C= (n.277+1545C=) c.*757C= (n.*757C=) c.1713C= (p.Asp571=) | |
| 16 | g.89935123C>G | CA397475088 | TUBB3 | c.672C>G (p.Asp224Glu) n.4093C>G c.456C>G (p.Asp152Glu) c.277+1545C>G (n.277+1545C>G) c.*757C>G (n.*757C>G) c.1713C>G (p.Asp571Glu) | |
| 16 | g.89935123C>T | CA8256149 | TUBB3 | c.672C>T (p.Asp224=) n.4093C>T c.456C>T (p.Asp152=) c.277+1545C>T (n.277+1545C>T) c.*757C>T (n.*757C>T) c.1713C>T (p.Asp571=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935124C>A | CA397475089 | TUBB3 | c.673C>A (p.Leu225Ile) n.4094C>A c.457C>A (p.Leu153Ile) c.277+1546C>A (n.277+1546C>A) c.*758C>A (n.*758C>A) c.1714C>A (p.Leu572Ile) | |
| 16 | g.89935124C>G | CA397475090 | TUBB3 | c.673C>G (p.Leu225Val) n.4094C>G c.457C>G (p.Leu153Val) c.277+1546C>G (n.277+1546C>G) c.*758C>G (n.*758C>G) c.1714C>G (p.Leu572Val) | |
| 16 | g.89935124C>T | CA397475091 | TUBB3 | c.673C>T (p.Leu225Phe) n.4094C>T c.457C>T (p.Leu153Phe) c.277+1546C>T (n.277+1546C>T) c.*758C>T (n.*758C>T) c.1714C>T (p.Leu572Phe) | ClinVar |
| 16 | g.89935125T>A | CA397475092 | TUBB3 | c.674T>A (p.Leu225His) n.4095T>A c.458T>A (p.Leu153His) c.277+1547T>A (n.277+1547T>A) c.*759T>A (n.*759T>A) c.1715T>A (p.Leu572His) | gnomAD v4 |
| 16 | g.89935125T>C | CA397475093 | TUBB3 | c.674T>C (p.Leu225Pro) n.4095T>C c.458T>C (p.Leu153Pro) c.277+1547T>C (n.277+1547T>C) c.*759T>C (n.*759T>C) c.1715T>C (p.Leu572Pro) | |
| 16 | g.89935125T>G | CA397475094 | TUBB3 | c.674T>G (p.Leu225Arg) n.4095T>G c.458T>G (p.Leu153Arg) c.277+1547T>G (n.277+1547T>G) c.*759T>G (n.*759T>G) c.1715T>G (p.Leu572Arg) | |
| 16 | g.89935126C>A | CA497381057 | TUBB3 | c.675C>A (p.Leu225=) n.4096C>A c.459C>A (p.Leu153=) c.277+1548C>A (n.277+1548C>A) c.*760C>A (n.*760C>A) c.1716C>A (p.Leu572=) | |
| 16 | g.89935126C>G | CA497381059 | TUBB3 | c.675C>G (p.Leu225=) n.4096C>G c.459C>G (p.Leu153=) c.277+1548C>G (n.277+1548C>G) c.*760C>G (n.*760C>G) c.1716C>G (p.Leu572=) | |
| 16 | g.89935126C>T | CA497381060 | TUBB3 | c.675C>T (p.Leu225=) n.4096C>T c.459C>T (p.Leu153=) c.277+1548C>T (n.277+1548C>T) c.*760C>T (n.*760C>T) c.1716C>T (p.Leu572=) | gnomAD v4 |
| 16 | g.89935127A>C | CA397475097 | TUBB3 | c.676A>C (p.Asn226His) n.4097A>C c.460A>C (p.Asn154His) c.277+1549A>C (n.277+1549A>C) c.*761A>C (n.*761A>C) c.1717A>C (p.Asn573His) | |
| 16 | g.89935127A>G | CA397475096 | TUBB3 | c.676A>G (p.Asn226Asp) n.4097A>G c.460A>G (p.Asn154Asp) c.277+1549A>G (n.277+1549A>G) c.*761A>G (n.*761A>G) c.1717A>G (p.Asn573Asp) | |
| 16 | g.89935127A>T | CA397475095 | TUBB3 | c.676A>T (p.Asn226Tyr) n.4097A>T c.460A>T (p.Asn154Tyr) c.277+1549A>T (n.277+1549A>T) c.*761A>T (n.*761A>T) c.1717A>T (p.Asn573Tyr) | |
| 16 | g.89935128A= | CA2242019950 | TUBB3 | c.677A= (p.Asn226=) n.4098A= c.461A= (p.Asn154=) c.277+1550A= (n.277+1550A=) c.*762A= (n.*762A=) c.1718A= (p.Asn573=) | |
| 16 | g.89935128A>C | CA397475098 | TUBB3 | c.677A>C (p.Asn226Thr) n.4098A>C c.461A>C (p.Asn154Thr) c.277+1550A>C (n.277+1550A>C) c.*762A>C (n.*762A>C) c.1718A>C (p.Asn573Thr) | |
| 16 | g.89935128A>G | CA397475099 | TUBB3 | c.677A>G (p.Asn226Ser) n.4098A>G c.461A>G (p.Asn154Ser) c.277+1550A>G (n.277+1550A>G) c.*762A>G (n.*762A>G) c.1718A>G (p.Asn573Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89935128A>T | CA397475100 | TUBB3 | c.677A>T (p.Asn226Ile) n.4098A>T c.461A>T (p.Asn154Ile) c.277+1550A>T (n.277+1550A>T) c.*762A>T (n.*762A>T) c.1718A>T (p.Asn573Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935129C>A | CA397475101 | TUBB3 | c.678C>A (p.Asn226Lys) n.4099C>A c.462C>A (p.Asn154Lys) c.277+1551C>A (n.277+1551C>A) c.*763C>A (n.*763C>A) c.1719C>A (p.Asn573Lys) | gnomAD v4 |
| 16 | g.89935129C>G | CA397475102 | TUBB3 | c.678C>G (p.Asn226Lys) n.4099C>G c.462C>G (p.Asn154Lys) c.277+1551C>G (n.277+1551C>G) c.*763C>G (n.*763C>G) c.1719C>G (p.Asn573Lys) | |
| 16 | g.89935129C>T | CA497381064 | TUBB3 | c.678C>T (p.Asn226=) n.4099C>T c.462C>T (p.Asn154=) c.277+1551C>T (n.277+1551C>T) c.*763C>T (n.*763C>T) c.1719C>T (p.Asn573=) | |
| 16 | g.89935130C>A | CA397475103 | TUBB3 | c.679C>A (p.His227Asn) n.4100C>A c.463C>A (p.His155Asn) c.277+1552C>A (n.277+1552C>A) c.*764C>A (n.*764C>A) c.1720C>A (p.His574Asn) | |
| 16 | g.89935130C>G | CA397475104 | TUBB3 | c.679C>G (p.His227Asp) n.4100C>G c.463C>G (p.His155Asp) c.277+1552C>G (n.277+1552C>G) c.*764C>G (n.*764C>G) c.1720C>G (p.His574Asp) | |
| 16 | g.89935130C>T | CA397475105 | TUBB3 | c.679C>T (p.His227Tyr) n.4100C>T c.463C>T (p.His155Tyr) c.277+1552C>T (n.277+1552C>T) c.*764C>T (n.*764C>T) c.1720C>T (p.His574Tyr) | |
| 16 | g.89935131A>C | CA397475106 | TUBB3 | c.680A>C (p.His227Pro) n.4101A>C c.464A>C (p.His155Pro) c.277+1553A>C (n.277+1553A>C) c.*765A>C (n.*765A>C) c.1721A>C (p.His574Pro) | |
| 16 | g.89935131A>G | CA397475107 | TUBB3 | c.680A>G (p.His227Arg) n.4101A>G c.464A>G (p.His155Arg) c.277+1553A>G (n.277+1553A>G) c.*765A>G (n.*765A>G) c.1721A>G (p.His574Arg) | ClinVar |
| 16 | g.89935131A>T | CA397475108 | TUBB3 | c.680A>T (p.His227Leu) n.4101A>T c.464A>T (p.His155Leu) c.277+1553A>T (n.277+1553A>T) c.*765A>T (n.*765A>T) c.1721A>T (p.His574Leu) | |
| 16 | g.89935132C>A | CA397475109 | TUBB3 | c.681C>A (p.His227Gln) n.4102C>A c.465C>A (p.His155Gln) c.277+1554C>A (n.277+1554C>A) c.*766C>A (n.*766C>A) c.1722C>A (p.His574Gln) | |
| 16 | g.89935132C>G | CA397475110 | TUBB3 | c.681C>G (p.His227Gln) n.4102C>G c.465C>G (p.His155Gln) c.277+1554C>G (n.277+1554C>G) c.*766C>G (n.*766C>G) c.1722C>G (p.His574Gln) | |
| 16 | g.89935132C>T | CA497381071 | TUBB3 | c.681C>T (p.His227=) n.4102C>T c.465C>T (p.His155=) c.277+1554C>T (n.277+1554C>T) c.*766C>T (n.*766C>T) c.1722C>T (p.His574=) | COSMIC |
| 16 | g.89935133C>A | CA397475112 | TUBB3 | c.682C>A (p.Leu228Met) n.4103C>A c.466C>A (p.Leu156Met) c.277+1555C>A (n.277+1555C>A) c.*767C>A (n.*767C>A) c.1723C>A (p.Leu575Met) | |
| 16 | g.89935133C>G | CA397475111 | TUBB3 | c.682C>G (p.Leu228Val) n.4103C>G c.466C>G (p.Leu156Val) c.277+1555C>G (n.277+1555C>G) c.*767C>G (n.*767C>G) c.1723C>G (p.Leu575Val) | |
| 16 | g.89935133C>T | CA497381073 | TUBB3 | c.682C>T (p.Leu228=) n.4103C>T c.466C>T (p.Leu156=) c.277+1555C>T (n.277+1555C>T) c.*767C>T (n.*767C>T) c.1723C>T (p.Leu575=) | gnomAD v4 |
| 16 | g.89935134T>A | CA397475113 | TUBB3 | c.683T>A (p.Leu228Gln) n.4104T>A c.467T>A (p.Leu156Gln) c.277+1556T>A (n.277+1556T>A) c.*768T>A (n.*768T>A) c.1724T>A (p.Leu575Gln) | |
| 16 | g.89935134T>C | CA397475114 | TUBB3 | c.683T>C (p.Leu228Pro) n.4104T>C c.467T>C (p.Leu156Pro) c.277+1556T>C (n.277+1556T>C) c.*768T>C (n.*768T>C) c.1724T>C (p.Leu575Pro) | ClinVar |
| 16 | g.89935134T>G | CA397475115 | TUBB3 | c.683T>G (p.Leu228Arg) n.4104T>G c.467T>G (p.Leu156Arg) c.277+1556T>G (n.277+1556T>G) c.*768T>G (n.*768T>G) c.1724T>G (p.Leu575Arg) | |
| 16 | g.89935135G>A | CA497381078 | TUBB3 | c.684G>A (p.Leu228=) n.4105G>A c.468G>A (p.Leu156=) c.277+1557G>A (n.277+1557G>A) c.*769G>A (n.*769G>A) c.1725G>A (p.Leu575=) | gnomAD v4 |
| 16 | g.89935135G>C | CA8256150 | TUBB3 | c.684G>C (p.Leu228=) n.4105G>C c.468G>C (p.Leu156=) c.277+1557G>C (n.277+1557G>C) c.*769G>C (n.*769G>C) c.1725G>C (p.Leu575=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935135G= | CA2242019952 | TUBB3 | c.684G= (p.Leu228=) n.4105G= c.468G= (p.Leu156=) c.277+1557G= (n.277+1557G=) c.*769G= (n.*769G=) c.1725G= (p.Leu575=) | |
| 16 | g.89935135G>T | CA497381080 | TUBB3 | c.684G>T (p.Leu228=) n.4105G>T c.468G>T (p.Leu156=) c.277+1557G>T (n.277+1557G>T) c.*769G>T (n.*769G>T) c.1725G>T (p.Leu575=) | |
| 16 | g.89935136G>A | CA397475116 | TUBB3 | c.685G>A (p.Val229Ile) n.4106G>A c.469G>A (p.Val157Ile) c.277+1558G>A (n.277+1558G>A) c.*770G>A (n.*770G>A) c.1726G>A (p.Val576Ile) | |
| 16 | g.89935136G>C | CA397475117 | TUBB3 | c.685G>C (p.Val229Leu) n.4106G>C c.469G>C (p.Val157Leu) c.277+1558G>C (n.277+1558G>C) c.*770G>C (n.*770G>C) c.1726G>C (p.Val576Leu) | |
| 16 | g.89935136G>T | CA397475118 | TUBB3 | c.685G>T (p.Val229Leu) n.4106G>T c.469G>T (p.Val157Leu) c.277+1558G>T (n.277+1558G>T) c.*770G>T (n.*770G>T) c.1726G>T (p.Val576Leu) | |
| 16 | g.89935137T>A | CA397475119 | TUBB3 | c.686T>A (p.Val229Glu) n.4107T>A c.470T>A (p.Val157Glu) c.277+1559T>A (n.277+1559T>A) c.*771T>A (n.*771T>A) c.1727T>A (p.Val576Glu) | |
| 16 | g.89935137T>C | CA397475120 | TUBB3 | c.686T>C (p.Val229Ala) n.4107T>C c.470T>C (p.Val157Ala) c.277+1559T>C (n.277+1559T>C) c.*771T>C (n.*771T>C) c.1727T>C (p.Val576Ala) | |
| 16 | g.89935137T>G | CA397475121 | TUBB3 | c.686T>G (p.Val229Gly) n.4107T>G c.470T>G (p.Val157Gly) c.277+1559T>G (n.277+1559T>G) c.*771T>G (n.*771T>G) c.1727T>G (p.Val576Gly) | |
| 16 | g.89935138A= | CA2242019959 | TUBB3 | c.687A= (p.Val229=) n.4108A= c.471A= (p.Val157=) c.277+1560A= (n.277+1560A=) c.*772A= (n.*772A=) c.1728A= (p.Val576=) | |
| 16 | g.89935138A>C | CA497381083 | TUBB3 | c.687A>C (p.Val229=) n.4108A>C c.471A>C (p.Val157=) c.277+1560A>C (n.277+1560A>C) c.*772A>C (n.*772A>C) c.1728A>C (p.Val576=) | |
| 16 | g.89935138A>G | CA286619078 | TUBB3 | c.687A>G (p.Val229=) n.4108A>G c.471A>G (p.Val157=) c.277+1560A>G (n.277+1560A>G) c.*772A>G (n.*772A>G) c.1728A>G (p.Val576=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935138A>T | CA8256151 | TUBB3 | c.687A>T (p.Val229=) n.4108A>T c.471A>T (p.Val157=) c.277+1560A>T (n.277+1560A>T) c.*772A>T (n.*772A>T) c.1728A>T (p.Val576=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935139T>A | CA397475124 | TUBB3 | c.688T>A (p.Ser230Thr) n.4109T>A c.472T>A (p.Ser158Thr) c.277+1561T>A (n.277+1561T>A) c.*773T>A (n.*773T>A) c.1729T>A (p.Ser577Thr) | |
| 16 | g.89935139T>C | CA397475123 | TUBB3 | c.688T>C (p.Ser230Pro) n.4109T>C c.472T>C (p.Ser158Pro) c.277+1561T>C (n.277+1561T>C) c.*773T>C (n.*773T>C) c.1729T>C (p.Ser577Pro) | |
| 16 | g.89935139T>G | CA397475122 | TUBB3 | c.688T>G (p.Ser230Ala) n.4109T>G c.472T>G (p.Ser158Ala) c.277+1561T>G (n.277+1561T>G) c.*773T>G (n.*773T>G) c.1729T>G (p.Ser577Ala) | |
| 16 | g.89935140C>A | CA397475125 | TUBB3 | c.689C>A (p.Ser230Ter) n.4110C>A c.473C>A (p.Ser158Ter) c.277+1562C>A (n.277+1562C>A) c.*774C>A (n.*774C>A) c.1730C>A (p.Ser577Ter) | |
| 16 | g.89935140C= | CA2242019967 | TUBB3 | c.689C= (p.Ser230=) n.4110C= c.473C= (p.Ser158=) c.277+1562C= (n.277+1562C=) c.*774C= (n.*774C=) c.1730C= (p.Ser577=) | |
| 16 | g.89935140C>G | CA397475126 | TUBB3 | c.689C>G (p.Ser230Trp) n.4110C>G c.473C>G (p.Ser158Trp) c.277+1562C>G (n.277+1562C>G) c.*774C>G (n.*774C>G) c.1730C>G (p.Ser577Trp) | |
| 16 | g.89935140C>T | CA10603568 | TUBB3 | c.689C>T (p.Ser230Leu) n.4110C>T c.473C>T (p.Ser158Leu) c.277+1562C>T (n.277+1562C>T) c.*774C>T (n.*774C>T) c.1730C>T (p.Ser577Leu) | ClinVar dbSNP |
| 16 | g.89935141G>A | CA8256152 | TUBB3 | c.690G>A (p.Ser230=) n.4111G>A c.474G>A (p.Ser158=) c.277+1563G>A (n.277+1563G>A) c.*775G>A (n.*775G>A) c.1731G>A (p.Ser577=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935141G>C | CA497381089 | TUBB3 | c.690G>C (p.Ser230=) n.4111G>C c.474G>C (p.Ser158=) c.277+1563G>C (n.277+1563G>C) c.*775G>C (n.*775G>C) c.1731G>C (p.Ser577=) | |
| 16 | g.89935141G= | CA2242019971 | TUBB3 | c.690G= (p.Ser230=) n.4111G= c.474G= (p.Ser158=) c.277+1563G= (n.277+1563G=) c.*775G= (n.*775G=) c.1731G= (p.Ser577=) | |
| 16 | g.89935141G>T | CA497381088 | TUBB3 | c.690G>T (p.Ser230=) n.4111G>T c.474G>T (p.Ser158=) c.277+1563G>T (n.277+1563G>T) c.*775G>T (n.*775G>T) c.1731G>T (p.Ser577=) | |
| 16 | g.89935142G>A | CA397475127 | TUBB3 | c.691G>A (p.Ala231Thr) n.4112G>A c.475G>A (p.Ala159Thr) c.277+1564G>A (n.277+1564G>A) c.*776G>A (n.*776G>A) c.1732G>A (p.Ala578Thr) | |
| 16 | g.89935142G>C | CA397475128 | TUBB3 | c.691G>C (p.Ala231Pro) n.4112G>C c.475G>C (p.Ala159Pro) c.277+1564G>C (n.277+1564G>C) c.*776G>C (n.*776G>C) c.1732G>C (p.Ala578Pro) | |
| 16 | g.89935142G>T | CA397475129 | TUBB3 | c.691G>T (p.Ala231Ser) n.4112G>T c.475G>T (p.Ala159Ser) c.277+1564G>T (n.277+1564G>T) c.*776G>T (n.*776G>T) c.1732G>T (p.Ala578Ser) | |
| 16 | g.89935143C>A | CA397475130 | TUBB3 | c.692C>A (p.Ala231Asp) n.4113C>A c.476C>A (p.Ala159Asp) c.277+1565C>A (n.277+1565C>A) c.*777C>A (n.*777C>A) c.1733C>A (p.Ala578Asp) | |
| 16 | g.89935143C= | CA2242019975 | TUBB3 | c.692C= (p.Ala231=) n.4113C= c.476C= (p.Ala159=) c.277+1565C= (n.277+1565C=) c.*777C= (n.*777C=) c.1733C= (p.Ala578=) | |
| 16 | g.89935143C>G | CA397475131 | TUBB3 | c.692C>G (p.Ala231Gly) n.4113C>G c.476C>G (p.Ala159Gly) c.277+1565C>G (n.277+1565C>G) c.*777C>G (n.*777C>G) c.1733C>G (p.Ala578Gly) | dbSNP |
| 16 | g.89935143C>T | CA397475132 | TUBB3 | c.692C>T (p.Ala231Val) n.4113C>T c.476C>T (p.Ala159Val) c.277+1565C>T (n.277+1565C>T) c.*777C>T (n.*777C>T) c.1733C>T (p.Ala578Val) | |
| 16 | g.89935144C>A | CA8256153 | TUBB3 | c.693C>A (p.Ala231=) n.4114C>A c.477C>A (p.Ala159=) c.277+1566C>A (n.277+1566C>A) c.*778C>A (n.*778C>A) c.1734C>A (p.Ala578=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935144C= | CA2242019977 | TUBB3 | c.693C= (p.Ala231=) n.4114C= c.477C= (p.Ala159=) c.277+1566C= (n.277+1566C=) c.*778C= (n.*778C=) c.1734C= (p.Ala578=) | |
| 16 | g.89935144C>G | CA497381093 | TUBB3 | c.693C>G (p.Ala231=) n.4114C>G c.477C>G (p.Ala159=) c.277+1566C>G (n.277+1566C>G) c.*778C>G (n.*778C>G) c.1734C>G (p.Ala578=) | |
| 16 | g.89935144C>T | CA497381095 | TUBB3 | c.693C>T (p.Ala231=) n.4114C>T c.477C>T (p.Ala159=) c.277+1566C>T (n.277+1566C>T) c.*778C>T (n.*778C>T) c.1734C>T (p.Ala578=) | gnomAD v4 |
| 16 | g.89935145A>C | CA397475133 | TUBB3 | c.694A>C (p.Thr232Pro) n.4115A>C c.478A>C (p.Thr160Pro) c.277+1567A>C (n.277+1567A>C) c.*779A>C (n.*779A>C) c.1735A>C (p.Thr579Pro) | |
| 16 | g.89935145A>G | CA397475134 | TUBB3 | c.694A>G (p.Thr232Ala) n.4115A>G c.478A>G (p.Thr160Ala) c.277+1567A>G (n.277+1567A>G) c.*779A>G (n.*779A>G) c.1735A>G (p.Thr579Ala) | |
| 16 | g.89935145A>T | CA397475135 | TUBB3 | c.694A>T (p.Thr232Ser) n.4115A>T c.478A>T (p.Thr160Ser) c.277+1567A>T (n.277+1567A>T) c.*779A>T (n.*779A>T) c.1735A>T (p.Thr579Ser) |