Colon Cancer: Gene >> QPCT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338415
Start	37359836:37359836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524A>G
AA Mutation	p.Asp175Gly(p.D175G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338415
Start	37372705:37372705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779100301
CDS Mutation	c.964C>T
AA Mutation	p.Pro322Ser(p.P322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338415
Start	37359593:37359593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116518028
CDS Mutation	c.281G>A
AA Mutation	p.Arg94Gln(p.R94Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338415
Start	37369732:37369732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338415
Start	37352806:37352806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338415
Start	37367360:37367360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338415
Start	37344811:37344811(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.85delG
AA Mutation	p.Val29SerfsTer20(p.V29Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338415
Start	37369737:37369738(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.783dupT
AA Mutation	p.Pro262SerfsTer14(p.P262Sfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> QPCT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338415
Start	37359744:37359744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432G>T
AA Mutation	p.Lys144Asn(p.K144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338415
Start	37369770:37369770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>T
AA Mutation	p.Arg270Ile(p.R270I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript