Colon Cancer: Gene >> INHA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243786
Start	219575297:219575297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872G>A
AA Mutation	p.Cys291Tyr(p.C291Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243786
Start	219574796:219574796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540215120
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243786
Start	219572556:219572556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182G>T
AA Mutation	p.Arg61Ile(p.R61I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243786
Start	219575248:219575248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823G>T
AA Mutation	p.Gly275Cys(p.G275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243786
Start	219575339:219575339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914T>G
AA Mutation	p.Leu305Arg(p.L305R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243786
Start	219575061:219575061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752787964
CDS Mutation	c.636G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243786
Start	219572500:219572500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243786
Start	219572494:219572494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243786
Start	219572566:219572566(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.197delG
AA Mutation	p.Gly66AlafsTer61(p.G66Afs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243786
Start	219574978:219574979(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.562_563dupCT
AA Mutation	p.Leu189CysfsTer2(p.L189Cfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> INHA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243786
Start	219575219:219575219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794T>C
AA Mutation	p.Val265Ala(p.V265A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243786
Start	219572548:219572548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243786
Start	219574978:219574979(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.562_563dupCT
AA Mutation	p.Leu189CysfsTer2(p.L189Cfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript