Colon Cancer: Gene >> CACUL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369151
Start	118754414:118754414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349A>C
AA Mutation	p.Thr117Pro(p.T117P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369151
Start	118754734:118754734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>A
AA Mutation	p.Gly10Glu(p.G10E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369151
Start	118701386:118701386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716A>T
AA Mutation	p.Lys239Met(p.K239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369151
Start	118691301:118691301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989A>C
AA Mutation	p.Lys330Thr(p.K330T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369151
Start	118729314:118729314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578G>C
AA Mutation	p.Arg193Thr(p.R193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369151
Start	118729335:118729335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.557delA
AA Mutation	p.Lys186ArgfsTer2(p.K186Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369151
Start	118686137:118686137(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1101delG
AA Mutation	p.Tyr368ThrfsTer100(p.Y368Tfs*100)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369151
Start	118691270:118691270(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1020delT
AA Mutation	p.Phe340LeufsTer128(p.F340Lfs*128)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000369151
Start	118691264:118691264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000369151
Start	118729387:118729388(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.504_505insTCC
AA Mutation	p.Tyr168_Lys169insSer(p.Y168_K169insS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CACUL1

No Mutation Annotation!