Colon Cancer: Gene >> CDC5L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371477
Start	44429878:44429878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2059G>A
AA Mutation	p.Asp687Asn(p.D687N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371477
Start	44446638:44446638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2336A>G
AA Mutation	p.Glu779Gly(p.E779G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371477
Start	44429750:44429750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1931A>C
AA Mutation	p.Lys644Thr(p.K644T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371477
Start	44445857:44445857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765Gln(p.R765Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371477
Start	44426549:44426549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718A>C
AA Mutation	p.Glu573Ala(p.E573A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371477
Start	44408615:44408615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075C>G
AA Mutation	p.Gln359Glu(p.Q359E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371477
Start	44429835:44429835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2016T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371477
Start	44403950:44403950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371477
Start	44426162:44426162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1629A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371477
Start	44403919:44403919(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.656delA
AA Mutation	p.Lys219SerfsTer24(p.K219Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371477
Start	44403938:44403938(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.673delT
AA Mutation	p.Tyr225MetfsTer18(p.Y225Mfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000371477
Start	44445823:44445823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2260G>T
AA Mutation	p.Glu754Ter(p.E754*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000371477
Start	44429774:44429775(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1955_1956insTTAGAAGACTAATTTTTTCC
AA Mutation	p.Ser653Ter(p.S653*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371477
Start	44406376:44406377(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.812_813insC
AA Mutation	p.Lys271AsnfsTer4(p.K271Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371477
Start	44408614:44408615(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1074_1075insTG
AA Mutation	p.Gln359CysfsTer22(p.Q359Cfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000371477
Start	44422652:44422654(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774713343
CDS Mutation	c.1249_1251delTCT
AA Mutation	p.Ser417del(p.S417del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDC5L

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000371477
Start	44426563:44426563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732G>T
AA Mutation	p.Glu578Ter(p.E578*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript