Colon Cancer: Gene >> CCDC18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93207238:93207238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049A>C
AA Mutation	p.Lys350Thr(p.K350T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93217752:93217752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842G>T
AA Mutation	p.Lys614Asn(p.K614N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93214757:93214757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507G>T
AA Mutation	p.Asp503Tyr(p.D503Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93216732:93216732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755044272
CDS Mutation	c.1813G>C
AA Mutation	p.Glu605Gln(p.E605Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93216723:93216723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804G>C
AA Mutation	p.Ala602Pro(p.A602P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93214833:93214833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1583G>T
AA Mutation	p.Arg528Leu(p.R528L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93232492:93232492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200030282
CDS Mutation	c.2356G>A
AA Mutation	p.Val786Ile(p.V786I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343253
Start	93217836:93217836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1926A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343253
Start	93258873:93258873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3669T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343253
Start	93201959:93201959(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779262598
CDS Mutation	c.774delA
AA Mutation	p.Val259TrpfsTer15(p.V259Wfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000343253
Start	93246106:93246106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2980G>T
AA Mutation	p.Glu994Ter(p.E994*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000343253
Start	93246902:93246902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3143T>G
AA Mutation	p.Leu1048Ter(p.L1048*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000343253
Start	93210891:93210891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299C>A
AA Mutation	p.Cys433Ter(p.C433*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000343253
Start	93214835:93214836(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1585_1586insAATAGTTGAAAGATTTAGT
AA Mutation	p.Thr529LysfsTer2(p.T529Kfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343253
Start	93216715:93216716(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1802dupA
AA Mutation	p.Asn601LysfsTer13(p.N601Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343253
Start	93193738:93193739(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.697dupA
AA Mutation	p.Arg233LysfsTer3(p.R233Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343253
Start	93217752:93217752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842G>T
AA Mutation	p.Lys614Asn(p.K614N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript