Colon Cancer: Gene >> GSK3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222330
Start	42239990:42239990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>A
AA Mutation	p.Ala146Thr(p.A146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222330
Start	42234409:42234409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848G>A
AA Mutation	p.Arg283His(p.R283H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222330
Start	42232625:42232625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156T>C
AA Mutation	p.Tyr386His(p.Y386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222330
Start	42233290:42233290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998T>C
AA Mutation	p.Ile333Thr(p.I333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222330
Start	42232662:42232662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201146173
CDS Mutation	c.1119G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222330
Start	42232590:42232590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222330
Start	42234633:42234634(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.711_712delCC
AA Mutation	p.Gln238GlyfsTer17(p.Q238Gfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222330
Start	42233198:42233198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1010delG
AA Mutation	p.Gly337GlufsTer11(p.G337Efs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000222330
Start	42233175:42233175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Ter(p.R345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GSK3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222330
Start	42232666:42232666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115C>T
AA Mutation	p.Thr372Met(p.T372M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222330
Start	42230851:42230851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372575967
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000222330
Start	42240080:42240080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>T
AA Mutation	p.Glu116Ter(p.E116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript