Colon Cancer: Gene >> DEPDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68482078:68482078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1730T>G
AA Mutation	p.Leu577Arg(p.L577R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68482289:68482289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519C>T
AA Mutation	p.Leu507Phe(p.L507F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68489012:68489012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494A>C
AA Mutation	p.His165Pro(p.H165P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68489528:68489528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395A>T
AA Mutation	p.Lys132Ile(p.K132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68494599:68494599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145G>T
AA Mutation	p.Ala49Ser(p.A49S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68489018:68489018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488T>A
AA Mutation	p.Ile163Lys(p.I163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68482724:68482724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084A>G
AA Mutation	p.Thr362Ala(p.T362A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68479308:68479308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1948T>C
AA Mutation	p.Phe650Leu(p.F650L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68482414:68482414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394T>G
AA Mutation	p.Phe465Cys(p.F465C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68479316:68479316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940T>C
AA Mutation	p.Ile647Thr(p.I647T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68482511:68482511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297T>G
AA Mutation	p.Ser433Ala(p.S433A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000456315
Start	68479207:68479207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2049T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DEPDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68477795:68477795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2290C>A
AA Mutation	p.Leu764Ile(p.L764I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68482084:68482084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1724C>A
AA Mutation	p.Ser575Tyr(p.S575Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68479238:68479238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2018C>A
AA Mutation	p.Ser673Tyr(p.S673Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68489490:68489490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777754199
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Cys(p.R145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000456315
Start	68489019:68489019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487A>G
AA Mutation	p.Ile163Val(p.I163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript