Colon Cancer: Gene >> CCDC116

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21635073:21635073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755475376
CDS Mutation	c.1010C>T
AA Mutation	p.Pro337Leu(p.P337L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21634227:21634227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758808128
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21634058:21634058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762931042
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Trp(p.R37W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21634161:21634161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760362089
CDS Mutation	c.212G>A
AA Mutation	p.Gly71Asp(p.G71D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21636685:21636685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457G>A
AA Mutation	p.Arg486His(p.R486H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21635060:21635060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749932957
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Cys(p.R333C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21634491:21634491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542A>G
AA Mutation	p.Gln181Arg(p.Q181R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21634859:21634859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796A>G
AA Mutation	p.Ile266Val(p.I266V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21636754:21636754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766787010
CDS Mutation	c.1526G>A
AA Mutation	p.Arg509Gln(p.R509Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21636588:21636588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141137219
CDS Mutation	c.1360G>A
AA Mutation	p.Glu454Lys(p.E454K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292779
Start	21634456:21634456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292779
Start	21636659:21636659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292779
Start	21635220:21635220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1161delC
AA Mutation	p.Ser388ProfsTer52(p.S388Pfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292779
Start	21634156:21634157(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.210dupT
AA Mutation	p.Gly71TrpfsTer9(p.G71Wfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC116

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292779
Start	21634446:21634446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497C>T
AA Mutation	p.Ala166Val(p.A166V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript