Colon Cancer: Gene >> DLST

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334220
Start	74889899:74889899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>A
AA Mutation	p.Val93Ile(p.V93I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334220
Start	74893423:74893423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563480250
CDS Mutation	c.671G>A
AA Mutation	p.Arg224Gln(p.R224Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334220
Start	74881957:74881957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334220
Start	74882599:74882599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334220
Start	74892879:74892879(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.491delC
AA Mutation	p.Pro164GlnfsTer39(p.P164Qfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334220
Start	74892914:74892914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.527delC
AA Mutation	p.Pro176LeufsTer27(p.P176Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DLST

No Mutation Annotation!