Colon Cancer: Gene >> TUBB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935782:89935782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587784504
CDS Mutation	c.1331C>T
AA Mutation	p.Ser444Leu(p.S444L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935526:89935526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>A
AA Mutation	p.Arg359Ser(p.R359S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89934753:89934753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>T
AA Mutation	p.Trp101Leu(p.W101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89934813:89934813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89934935:89934935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935008:89935008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770484819
CDS Mutation	c.557C>T
AA Mutation	p.Thr186Met(p.T186M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89935432:89935432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775854497
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89935213:89935213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758044135
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89934985:89934985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143029958
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89935174:89935174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89934931:89934931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89935192:89935192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138498822
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000315491
Start	89935051:89935051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>G
AA Mutation	p.Tyr200Ter(p.Y200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TUBB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935527:89935527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529172770
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359His(p.R359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935590:89935590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777149755
CDS Mutation	c.1139G>A
AA Mutation	p.Arg380His(p.R380H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935179:89935179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587784506
CDS Mutation	c.728C>T
AA Mutation	p.Pro243Leu(p.P243L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935744:89935744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293G>T
AA Mutation	p.Glu431Asp(p.E431D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315491
Start	89935733:89935733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>A
AA Mutation	p.Ala428Thr(p.A428T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315491
Start	89935678:89935678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758588994
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript