Colon Cancer: Gene >> PIANP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6696516:6696516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532C>T
AA Mutation	p.Pro178Ser(p.P178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6697577:6697577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181795908
CDS Mutation	c.233G>A
AA Mutation	p.Arg78Gln(p.R78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6697317:6697317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529550863
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Trp(p.R165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6697730:6697730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>T
AA Mutation	p.Pro27Leu(p.P27L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6696470:6696470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578T>C
AA Mutation	p.Val193Ala(p.V193A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6695041:6695041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>A
AA Mutation	p.Leu282Met(p.L282M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320591
Start	6697405:6697406(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.404dupC
AA Mutation	p.His136SerfsTer16(p.H136Sfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PIANP

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000320591
Start	6696445:6696445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603C>A
AA Mutation	p.Phe201Leu(p.F201L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320591
Start	6697341:6697341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469C>A
AA Mutation	p.Leu157Ile(p.L157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript