Colon Cancer: Gene >> DPYSL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26624244:26624244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Val139Met(p.V139M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26634882:26634882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751569597
CDS Mutation	c.793G>A
AA Mutation	p.Ala265Thr(p.A265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26634891:26634891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Trp(p.R268W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26643486:26643486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>A
AA Mutation	p.Gly287Ser(p.G287S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26583872:26583872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>A
AA Mutation	p.Gly68Arg(p.G68R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26653296:26653296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374825617
CDS Mutation	c.1526C>T
AA Mutation	p.Thr509Met(p.T509M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26653307:26653307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1537G>A
AA Mutation	p.Val513Ile(p.V513I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26581976:26581976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765937076
CDS Mutation	c.47G>A
AA Mutation	p.Arg16His(p.R16H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26634892:26634892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311151
Start	26624267:26624267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760000083
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311151
Start	26627280:26627280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773335767
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311151
Start	26655668:26655668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1686delC
AA Mutation	p.Gly563ValfsTer121(p.G563Vfs*121)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DPYSL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26647768:26647768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771160273
CDS Mutation	c.1249G>A
AA Mutation	p.Val417Ile(p.V417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311151
Start	26647735:26647735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216G>A
AA Mutation	p.Asp406Asn(p.D406N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000311151
Start	26583888:26583908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.219_239delCACTCGTTTCCAGATGCCTGA
AA Mutation	p.Thr74_Asp80del(p.T74_D80del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript