Colon Cancer: Gene >> CCDC80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639253:112639253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653T>C
AA Mutation	p.Leu218Pro(p.L218P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112638506:112638506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400G>A
AA Mutation	p.Arg467His(p.R467H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112607227:112607227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2455T>A
AA Mutation	p.Leu819Ile(p.L819I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639879:112639879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27C>A
AA Mutation	p.Phe9Leu(p.F9L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112638755:112638755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139212823
CDS Mutation	c.1151C>T
AA Mutation	p.Thr384Met(p.T384M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639098:112639098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Glu270Lys(p.E270K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639112:112639112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794C>A
AA Mutation	p.Pro265His(p.P265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112605536:112605536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771980493
CDS Mutation	c.2734C>T
AA Mutation	p.Arg912Cys(p.R912C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639292:112639292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>A
AA Mutation	p.Ser205Asn(p.S205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639563:112639563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Cys(p.R115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639505:112639505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770365462
CDS Mutation	c.401C>T
AA Mutation	p.Ser134Leu(p.S134L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112610062:112610062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2341T>A
AA Mutation	p.Leu781Met(p.L781M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639116:112639116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790G>A
AA Mutation	p.Gly264Ser(p.G264S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639515:112639515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112605531:112605531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2739C>G
AA Mutation	p.Cys913Trp(p.C913W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112607227:112607227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2455T>G
AA Mutation	p.Leu819Val(p.L819V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112638987:112638987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919G>T
AA Mutation	p.Gly307Cys(p.G307C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112638618:112638618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288A>G
AA Mutation	p.Thr430Ala(p.T430A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206423
Start	112639294:112639294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206423
Start	112605654:112605654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777722433
CDS Mutation	c.2616C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206423
Start	112630129:112630129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206423
Start	112638982:112638982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000206423
Start	112607215:112607215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2467G>T
AA Mutation	p.Glu823Ter(p.E823*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000206423
Start	112638039:112638039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1867C>T
AA Mutation	p.Arg623Ter(p.R623*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112616827:112616827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2204C>A
AA Mutation	p.Ser735Tyr(p.S735Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112638926:112638926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980G>A
AA Mutation	p.Arg327Gln(p.R327Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112607251:112607251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2431C>T
AA Mutation	p.Arg811Cys(p.R811C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112638260:112638260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1646A>G
AA Mutation	p.Glu549Gly(p.E549G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000206423
Start	112639530:112639530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Trp(p.R126W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript