Colon Cancer: Gene >> IL25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23373323:23373323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375944472
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Cys(p.R69C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23375834:23375834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375340039
CDS Mutation	c.488G>A
AA Mutation	p.Arg163His(p.R163H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23375792:23375792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446A>C
AA Mutation	p.Lys149Thr(p.K149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23375692:23375692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144470149
CDS Mutation	c.346G>A
AA Mutation	p.Val116Ile(p.V116I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23375633:23375633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287G>T
AA Mutation	p.Arg96Ile(p.R96I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329715
Start	23375691:23375691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329715
Start	23375871:23375871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23373219:23373219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101G>A
AA Mutation	p.Ser34Asn(p.S34N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329715
Start	23375665:23375665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319C>G
AA Mutation	p.His107Asp(p.H107D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript