Colon Cancer: Gene >> TACC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38827217:38827217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502G>A
AA Mutation	p.Gly501Asp(p.G501D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38788789:38788789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247G>A
AA Mutation	p.Gly83Arg(p.G83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38820182:38820182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377342873
CDS Mutation	c.938C>T
AA Mutation	p.Ser313Leu(p.S313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38820265:38820265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021C>T
AA Mutation	p.Leu341Phe(p.L341F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38819743:38819743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141796337
CDS Mutation	c.499G>A
AA Mutation	p.Gly167Arg(p.G167R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38819998:38819998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759820712
CDS Mutation	c.754G>A
AA Mutation	p.Ala252Thr(p.A252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38820625:38820625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368667882
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Cys(p.R461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000317827
Start	38788706:38788706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771016874
CDS Mutation	c.164C>T
AA Mutation	p.Ser55Leu(p.S55L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38819731:38819731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487T>C
AA Mutation	p.Ser163Pro(p.S163P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317827
Start	38788707:38788707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317827
Start	38820466:38820473(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1222_1229delCCCCTCTC
AA Mutation	p.Pro408PhefsTer2(p.P408Ffs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TACC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38846725:38846725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749374701
CDS Mutation	c.2255G>A
AA Mutation	p.Arg752Gln(p.R752Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38825343:38825343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427C>A
AA Mutation	p.Ser476Tyr(p.S476Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38819819:38819819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575A>G
AA Mutation	p.Gln192Arg(p.Q192R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317827
Start	38820514:38820514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202236973
CDS Mutation	c.1270G>A
AA Mutation	p.Glu424Lys(p.E424K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000317827
Start	38820121:38820121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>T
AA Mutation	p.Glu293Ter(p.E293*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript