Colon Cancer: Gene >> TIAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436547
Start	119581985:119581985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308A>G
AA Mutation	p.Asp103Gly(p.D103G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000436547
Start	119576644:119576644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968G>T
AA Mutation	p.Gly323Val(p.G323V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000436547
Start	119579985:119579985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000436547
Start	119577715:119577715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578T>C
AA Mutation	p.Phe193Ser(p.F193S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000436547
Start	119582205:119582205(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	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436547
Start	119577729:119577729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436547
Start	119577682:119577682(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.611delA
AA Mutation	p.Asn204IlefsTer13(p.N204Ifs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436547
Start	119581989:119581990(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.303dupT
AA Mutation	p.Gly102TrpfsTer21(p.G102Wfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436547
Start	119582178:119582179(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.273dupA
AA Mutation	p.Asp92ArgfsTer31(p.D92Rfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TIAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436547
Start	119582471:119582471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216A>C
AA Mutation	p.Lys72Asn(p.K72N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript