Colon Cancer: Gene >> ERCC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300853
Start	45414905:45414905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000300853
Start	45414863:45414863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772941786
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Trp(p.R234W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300853
Start	45420373:45420373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374992813
CDS Mutation	c.376G>A
AA Mutation	p.Val126Ile(p.V126I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300853
Start	45419155:45419155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748656673
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300853
Start	45423327:45423327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300853
Start	45423306:45423307(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.62_68dupAATTTGT
AA Mutation	p.Pro25CysfsTer8(p.P25Cfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ERCC1

No Mutation Annotation!