Colon Cancer: Gene >> CCDC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263102
Start	59792939:59792939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403C>T
AA Mutation	p.Ala468Val(p.A468V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263102
Start	59812755:59812755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749668592
CDS Mutation	c.727C>T
AA Mutation	p.Pro243Ser(p.P243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263102
Start	59794564:59794564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139C>T
AA Mutation	p.Thr380Met(p.T380M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263102
Start	59793075:59793075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267T>A
AA Mutation	p.Phe423Ile(p.F423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263102
Start	59814749:59814749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Trp(p.R197W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263102
Start	59806930:59806930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762276135
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000263102
Start	59792994:59792994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>T
AA Mutation	p.Gln450Ter(p.Q450*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000263102
Start	59814653:59814653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746439006
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Ter(p.R229*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263102
Start	59806980:59806981(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.945_946insTACCAAA
AA Mutation	p.Glu316TyrfsTer13(p.E316Yfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263102
Start	59832593:59832594(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.513_514insTTAAAGCTTAAAAG
AA Mutation	p.Asn172LeufsTer8(p.N172Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263102
Start	59793113:59793113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000263102
Start	59852589:59852591(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.415_417delGAA
AA Mutation	p.Glu139del(p.E139del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000263102
Start	59806982:59806983(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.943_944insCAG
AA Mutation	p.Arg315delinsThrGly(p.R315delinsTG)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC6

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000263102
Start	59852678:59852678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>T
AA Mutation	p.Glu110Ter(p.E110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript