Colon Cancer: Gene >> DIS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72773778:72773778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139907646
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382Gln(p.R382Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72775945:72775945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373230191
CDS Mutation	c.802G>A
AA Mutation	p.Asp268Asn(p.D268N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72771860:72771860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540A>T
AA Mutation	p.Arg514Trp(p.R514W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72763512:72763512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066G>A
AA Mutation	p.Arg689Gln(p.R689Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72761809:72761809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348C>T
AA Mutation	p.Ala783Val(p.A783V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72773736:72773736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369590515
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396Gln(p.R396Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72761713:72761713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2444A>C
AA Mutation	p.Lys815Thr(p.K815T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72768860:72768860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1808A>C
AA Mutation	p.Asn603Thr(p.N603T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72761488:72761488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2545G>A
AA Mutation	p.Glu849Lys(p.E849K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72766003:72766003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1939G>A
AA Mutation	p.Asp647Asn(p.D647N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377767
Start	72771882:72771882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377767
Start	72772750:72772750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377767
Start	72761940:72761940(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2325delT
AA Mutation	p.Phe775LeufsTer30(p.F775Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DIS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72763512:72763512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066G>A
AA Mutation	p.Arg689Gln(p.R689Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72773778:72773778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139907646
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382Gln(p.R382Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72761783:72761783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2374G>A
AA Mutation	p.Ala792Thr(p.A792T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377767
Start	72761473:72761473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2560T>C
AA Mutation	p.Phe854Leu(p.F854L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377767
Start	72762012:72762012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2253T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000377767
Start	72777488:72777488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>T
AA Mutation	p.Glu196Ter(p.E196*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript