Colon Cancer: Gene >> COLQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15466370:15466370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201158622
CDS Mutation	c.785G>A
AA Mutation	p.Arg262His(p.R262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15456500:15456500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034C>A
AA Mutation	p.Ser345Tyr(p.S345Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15456527:15456527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007C>T
AA Mutation	p.Ala336Val(p.A336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15488261:15488261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266C>T
AA Mutation	p.Ser89Leu(p.S89L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15488214:15488214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201507876
CDS Mutation	c.313G>A
AA Mutation	p.Gly105Ser(p.G105S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383788
Start	15479353:15479353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383788
Start	15488260:15488260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144897863
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383788
Start	15455930:15455930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149852377
CDS Mutation	c.1164C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383788
Start	15456011:15456011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383788
Start	15521554:15521554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111339593
CDS Mutation	c.72G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383788
Start	15456574:15456574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.960delT
AA Mutation	p.Phe320LeufsTer12(p.F320Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000383788
Start	15479343:15479343(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	splice_acceptor_variant
Transcription ID	ENST00000383788
Start	15477198:15477198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000383788
Start	15455898:15455898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755782087
CDS Mutation	c.1195+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> COLQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15489580:15489580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774271810
CDS Mutation	c.164C>T
AA Mutation	p.Thr55Met(p.T55M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383788
Start	15474262:15474262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566G>T
AA Mutation	p.Gly189Val(p.G189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript