Colon Cancer: Gene >> UGT2B4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69485224:69485224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375061246
CDS Mutation	c.1294G>A
AA Mutation	p.Val432Ile(p.V432I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69480843:69480843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>A
AA Mutation	p.Ala460Thr(p.A460T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69480792:69480792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778378649
CDS Mutation	c.1429C>T
AA Mutation	p.Arg477Trp(p.R477W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69480689:69480689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532G>C
AA Mutation	p.Cys511Ser(p.C511S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69495657:69495657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767028471
CDS Mutation	c.205C>T
AA Mutation	p.Pro69Ser(p.P69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69495330:69495330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532T>C
AA Mutation	p.Tyr178His(p.Y178H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69480815:69480815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406G>A
AA Mutation	p.Arg469His(p.R469H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69489561:69489561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Glu294Lys(p.E294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69495247:69495247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>T
AA Mutation	p.Met205Ile(p.M205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69480777:69480777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767837637
CDS Mutation	c.1444G>A
AA Mutation	p.Asp482Asn(p.D482N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000305107
Start	69480908:69480908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1313A>C
AA Mutation	p.Tyr438Ser(p.Y438S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305107
Start	69495253:69495253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305107
Start	69495328:69495328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370531105
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000305107
Start	69489486:69489486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955G>T
AA Mutation	p.Glu319Ter(p.E319*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UGT2B4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69495186:69495186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676A>C
AA Mutation	p.Ile226Leu(p.I226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305107
Start	69495716:69495716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>T
AA Mutation	p.Arg49Ile(p.R49I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000305107
Start	69495525:69495525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>T
AA Mutation	p.Gln113Ter(p.Q113*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript