Colon Cancer: Gene >> CANT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302345
Start	78997193:78997193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302345
Start	78997579:78997579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44T>C
AA Mutation	p.Met15Thr(p.M15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302345
Start	78993701:78993701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055A>G
AA Mutation	p.Asn352Ser(p.N352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302345
Start	78997504:78997504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375819727
CDS Mutation	c.119G>A
AA Mutation	p.Arg40His(p.R40H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302345
Start	78993694:78993694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302345
Start	78993808:78993808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556238561
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302345
Start	78997413:78997413(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.210delC
AA Mutation	p.Thr71ProfsTer59(p.T71Pfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000302345
Start	78993826:78993828(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.928_930delAAG
AA Mutation	p.Lys310del(p.K310del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CANT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302345
Start	78993705:78993705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051C>A
AA Mutation	p.Pro351Thr(p.P351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript