Colon Cancer: Gene >> GAN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81377579:81377579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1777C>T
AA Mutation	p.Arg593Cys(p.R593C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81315256:81315256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143T>C
AA Mutation	p.Leu48Pro(p.L48P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81354670:81354670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>A
AA Mutation	p.Ser183Tyr(p.S183Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81356933:81356933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574374537
CDS Mutation	c.782C>T
AA Mutation	p.Ala261Val(p.A261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81354565:81354565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443A>G
AA Mutation	p.His148Arg(p.H148R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81377305:81377305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589A>T
AA Mutation	p.Tyr530Phe(p.Y530F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81356803:81356803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652A>G
AA Mutation	p.Met218Val(p.M218V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81354566:81354566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764605890
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81365359:81365359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147725941
CDS Mutation	c.1383G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81363889:81363889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150102659
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81363808:81363808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142479585
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81354456:81354456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000568107
Start	81357835:81357835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370358470
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Ter(p.R293*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000568107
Start	81365349:81365349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GAN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81354556:81354556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434G>A
AA Mutation	p.Cys145Tyr(p.C145Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000568107
Start	81377244:81377244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1528T>G
AA Mutation	p.Leu510Val(p.L510V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81354518:81354518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81357879:81357879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368910322
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81351640:81351640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568107
Start	81362518:81362518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199908897
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000568107
Start	81354723:81354723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs119485090
CDS Mutation	c.601C>T
AA Mutation	p.Arg201Ter(p.R201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript