Colon Cancer: Gene >> IRGC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719757:43719757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400His(p.R400H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719486:43719486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758855988
CDS Mutation	c.928G>A
AA Mutation	p.Asp310Asn(p.D310N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719549:43719549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991C>T
AA Mutation	p.Arg331Cys(p.R331C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43718986:43718986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56159111
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719640:43719640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082T>C
AA Mutation	p.Phe361Ser(p.F361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719045:43719045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487T>C
AA Mutation	p.Phe163Leu(p.F163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43718752:43718752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194C>T
AA Mutation	p.Ala65Val(p.A65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719018:43719018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749054115
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000244314
Start	43719166:43719166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756387844
CDS Mutation	c.608G>A
AA Mutation	p.Arg203Gln(p.R203Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43719890:43719890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73564645
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43718846:43718846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774670679
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43718822:43718822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541211616
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43719227:43719227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760760691
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43719482:43719482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565345774
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43719611:43719611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543218904
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRGC

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43719479:43719479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244314
Start	43719608:43719608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374269776
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript