Colon Cancer: Gene >> GAB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143438088:143438088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683G>A
AA Mutation	p.Ser228Asn(p.S228N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143415660:143415660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374885566
CDS Mutation	c.256G>T
AA Mutation	p.Asp86Tyr(p.D86Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143469169:143469169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2065C>T
AA Mutation	p.Pro689Ser(p.P689S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143415644:143415644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240A>C
AA Mutation	p.Glu80Asp(p.E80D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143433706:143433706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754987077
CDS Mutation	c.583G>A
AA Mutation	p.Glu195Lys(p.E195K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143415729:143415729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201202756
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Cys(p.R109C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143469110:143469110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006C>A
AA Mutation	p.Ala669Asp(p.A669D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143438384:143438384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979A>G
AA Mutation	p.Thr327Ala(p.T327A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262994
Start	143440124:143440124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262994
Start	143466189:143466189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262994
Start	143337232:143337232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777158611
CDS Mutation	c.50delC
AA Mutation	p.Pro17ArgfsTer5(p.P17Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000262994
Start	143438594:143438594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Ter(p.R397*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262994
Start	143415629:143415630(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.231dupA
AA Mutation	p.Glu78ArgfsTer3(p.E78Rfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GAB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262994
Start	143415664:143415664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763452007
CDS Mutation	c.260T>C
AA Mutation	p.Ile87Thr(p.I87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript