Colon Cancer: Gene >> DPYS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104429620:104429620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875C>T
AA Mutation	p.Ala292Val(p.A292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104392868:104392868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359C>A
AA Mutation	p.Phe453Leu(p.F453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000351513
Start	104392786:104392786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150948846
CDS Mutation	c.1441C>T
AA Mutation	p.Arg481Trp(p.R481W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104444409:104444409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632T>C
AA Mutation	p.Ile211Thr(p.I211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104424324:104424324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158T>A
AA Mutation	p.Phe386Leu(p.F386L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104447475:104447475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452A>G
AA Mutation	p.Gln151Arg(p.Q151R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104428009:104428009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559507379
CDS Mutation	c.1063C>T
AA Mutation	p.Arg355Trp(p.R355W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104447357:104447357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>T
AA Mutation	p.Gln190His(p.Q190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104447450:104447450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.477G>T
AA Mutation	p.Lys159Asn(p.K159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104381272:104381272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>A
AA Mutation	p.Glu496Lys(p.E496K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104444335:104444335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149927226
CDS Mutation	c.706A>G
AA Mutation	p.Ile236Val(p.I236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104392863:104392863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364T>A
AA Mutation	p.Val455Asp(p.V455D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104392972:104392972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255C>A
AA Mutation	p.His419Asn(p.H419N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104447355:104447355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572T>C
AA Mutation	p.Val191Ala(p.V191A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351513
Start	104427983:104427983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373819650
CDS Mutation	c.1089C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000351513
Start	104466886:104466886(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.35delG
AA Mutation	p.Gly12ValfsTer86(p.G12Vfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DPYS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104429618:104429618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.877G>A
AA Mutation	p.Ala293Thr(p.A293T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104447431:104447431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>T
AA Mutation	p.Asp166Tyr(p.D166Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351513
Start	104451287:104451287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533803158
CDS Mutation	c.382G>A
AA Mutation	p.Asp128Asn(p.D128N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript