Colon Cancer: Gene >> DAO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108899431:108899431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201364697
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Trp(p.R290W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108893014:108893014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775565169
CDS Mutation	c.485G>A
AA Mutation	p.Arg162Gln(p.R162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108885121:108885121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115T>G
AA Mutation	p.Phe39Val(p.F39V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108885040:108885040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373913310
CDS Mutation	c.34G>A
AA Mutation	p.Gly12Arg(p.G12R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108892993:108892993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464G>T
AA Mutation	p.Arg155Met(p.R155M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108894318:108894318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749872143
CDS Mutation	c.563C>T
AA Mutation	p.Ala188Val(p.A188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108885071:108885071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200257378
CDS Mutation	c.65G>A
AA Mutation	p.Arg22His(p.R22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108899411:108899411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143550642
CDS Mutation	c.848G>A
AA Mutation	p.Arg283Gln(p.R283Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108887467:108887467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212C>G
AA Mutation	p.Thr71Ser(p.T71S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228476
Start	108894355:108894355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228476
Start	108887519:108887519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000228476
Start	108889520:108889520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Glu121Ter(p.E121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000228476
Start	108885088:108885088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773218020
CDS Mutation	c.82C>T
AA Mutation	p.Gln28Ter(p.Q28*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DAO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108885142:108885142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375063129
CDS Mutation	c.136G>A
AA Mutation	p.Asp46Asn(p.D46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108900494:108900494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759096607
CDS Mutation	c.1003G>A
AA Mutation	p.Glu335Lys(p.E335K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228476
Start	108890233:108890233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412A>C
AA Mutation	p.Ile138Leu(p.I138L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript