Colon Cancer: Gene >> DPYSL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147400778:147400778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>A
AA Mutation	p.Ala342Thr(p.A342T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147418456:147418456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304A>G
AA Mutation	p.Thr102Ala(p.T102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147424941:147424941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62G>T
AA Mutation	p.Gly21Val(p.G21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147395693:147395693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490G>A
AA Mutation	p.Gly497Asp(p.G497D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147397674:147397674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747491194
CDS Mutation	c.1453C>T
AA Mutation	p.Arg485Trp(p.R485W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147401615:147401615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>T
AA Mutation	p.Ala298Val(p.A298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147399173:147399173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397His(p.R397H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398514
Start	147399123:147399123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240C>T
AA Mutation	p.Pro414Ser(p.P414S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147405695:147405695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147394056:147394056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147399190:147399190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398514
Start	147395638:147395638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1545delC
AA Mutation	p.Ala516GlnfsTer15(p.A516Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DPYSL3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398514
Start	147415746:147415746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761152983
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript