Colon Cancer: Gene >> GSK3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119876421:119876421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901T>C
AA Mutation	p.Trp301Arg(p.W301R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	120002228:120002228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>A
AA Mutation	p.Gly34Ser(p.G34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119916114:119916114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>T
AA Mutation	p.Arg180Trp(p.R180W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119863559:119863559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72548709
CDS Mutation	c.956G>A
AA Mutation	p.Arg319His(p.R319H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264235
Start	119912706:119912706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713T>C
AA Mutation	p.Ile238Thr(p.I238T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119923470:119923470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380A>G
AA Mutation	p.Tyr127Cys(p.Y127C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119923382:119923382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468T>G
AA Mutation	p.Ile156Met(p.I156M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119843324:119843324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126A>G
AA Mutation	p.Ile376Val(p.I376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	120002081:120002081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247G>A
AA Mutation	p.Ala83Thr(p.A83T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000264235
Start	119876475:119876475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847G>T
AA Mutation	p.Glu283Ter(p.E283*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000264235
Start	119863599:119863599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768552900
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Ter(p.R306*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GSK3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119863554:119863554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Met(p.L321M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119863592:119863592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775606264
CDS Mutation	c.923G>A
AA Mutation	p.Arg308Gln(p.R308Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	120093413:120093413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22A>T
AA Mutation	p.Thr8Ser(p.T8S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264235
Start	119843285:119843285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165T>C
AA Mutation	p.Ser389Pro(p.S389P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264235
Start	119826806:119826806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000264235
Start	120002090:120002090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238G>T
AA Mutation	p.Glu80Ter(p.E80*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript