Colon Cancer: Gene >> DAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49532215:49532215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704C>A
AA Mutation	p.Ser568Arg(p.S568R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49510800:49510800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266C>T
AA Mutation	p.Ser89Phe(p.S89F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49510760:49510760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772814756
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Cys(p.R76C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49532219:49532219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370669533
CDS Mutation	c.1708G>A
AA Mutation	p.Val570Met(p.V570M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49531880:49531880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544574838
CDS Mutation	c.1369C>T
AA Mutation	p.Arg457Trp(p.R457W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49533177:49533177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2666C>A
AA Mutation	p.Pro889His(p.P889H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49531106:49531106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595C>T
AA Mutation	p.Leu199Phe(p.L199F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49531852:49531852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49510813:49510813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49531072:49531072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.561T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49531846:49531846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762819634
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49531063:49531063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749602970
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49532068:49532068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201897321
CDS Mutation	c.1557G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308775
Start	49531764:49531764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1256delC
AA Mutation	p.Pro419LeufsTer88(p.P419Lfs*88)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308775
Start	49530871:49530871(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.364delC
AA Mutation	p.Asp123ThrfsTer11(p.D123Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49532011:49532011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1500G>T
AA Mutation	p.Lys500Asn(p.K500N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49510684:49510684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>A
AA Mutation	p.Met50Ile(p.M50I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308775
Start	49531622:49531622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62261248
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Trp(p.R371W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308775
Start	49533019:49533019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2508G>T
Mutation Classification	Silent
Feature Type	Transcript