Colon Cancer: Gene >> GAB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78226533:78226533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139G>T
AA Mutation	p.Arg380Ile(p.R380I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78226600:78226600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072C>T
AA Mutation	p.Pro358Ser(p.P358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78220437:78220437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1769C>G
AA Mutation	p.Pro590Arg(p.P590R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78220378:78220378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780858100
CDS Mutation	c.1828G>A
AA Mutation	p.Gly610Ser(p.G610S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361507
Start	78226482:78226482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190A>G
AA Mutation	p.Asn397Ser(p.N397S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78226817:78226817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755736799
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78221698:78221698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757341769
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361507
Start	78222161:78222161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361507
Start	78223444:78223444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1535delC
AA Mutation	p.Pro512LeufsTer19(p.P512Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GAB2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361507
Start	78225111:78225112(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1298_1299delTC
AA Mutation	p.Phe433SerfsTer16(p.F433Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript