Colon Cancer: Gene >> UGT1A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373409
Start	233719434:233719434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614T>C
AA Mutation	p.Met205Thr(p.M205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373409
Start	233718927:233718927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149779946
CDS Mutation	c.107C>T
AA Mutation	p.Thr36Ile(p.T36I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373409
Start	233719280:233719280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762367100
CDS Mutation	c.460G>A
AA Mutation	p.Val154Ile(p.V154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373409
Start	233719349:233719349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Pro177Ser(p.P177S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373409
Start	233719472:233719472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>G
AA Mutation	p.Leu218Val(p.L218V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373409
Start	233719331:233719331(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780658532
CDS Mutation	c.517delT
AA Mutation	p.Trp173GlyfsTer8(p.W173Gfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373409
Start	233719330:233719331(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.517dupT
AA Mutation	p.Trp173LeufsTer7(p.W173Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> UGT1A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373409
Start	233719152:233719152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>A
AA Mutation	p.Ser111Tyr(p.S111Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373409
Start	233719465:233719465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>G
Mutation Classification	Silent
Feature Type	Transcript