Colon Cancer: Gene >> INA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103278248:103278248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346Gln(p.R346Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103277453:103277453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242C>T
AA Mutation	p.Ala81Val(p.A81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103277482:103277482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760759982
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103288608:103288608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439C>A
AA Mutation	p.Ser480Tyr(p.S480Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103288385:103288385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757776233
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Cys(p.R406C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103278155:103278155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944A>T
AA Mutation	p.Tyr315Phe(p.Y315F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103288624:103288624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1455G>T
AA Mutation	p.Glu485Asp(p.E485D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103277824:103277824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>T
AA Mutation	p.Gly205Cys(p.G205C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369849
Start	103277955:103277955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369849
Start	103277877:103277877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369849
Start	103288659:103288659(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1495delA
AA Mutation	p.Ile499TyrfsTer15(p.I499Yfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000369849
Start	103288583:103288583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414G>T
AA Mutation	p.Glu472Ter(p.E472*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> INA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103287066:103287066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097G>T
AA Mutation	p.Arg366Met(p.R366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369849
Start	103287110:103287110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141G>T
AA Mutation	p.Asp381Tyr(p.D381Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000369849
Start	103288640:103288640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471G>T
AA Mutation	p.Glu491Ter(p.E491*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript