Colon Cancer: Gene >> SSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244763
Start	7289922:7289922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803C>T
AA Mutation	p.Ser268Leu(p.S268L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000244763
Start	7298747:7298747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777732061
CDS Mutation	c.620C>T
AA Mutation	p.Thr207Ile(p.T207I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244763
Start	7309943:7309943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166G>C
AA Mutation	p.Val56Leu(p.V56L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244763
Start	7301357:7301357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Gly166Arg(p.G166R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244763
Start	7298780:7298780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587T>G
AA Mutation	p.Val196Gly(p.V196G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000244763
Start	7310000:7310000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109G>T
AA Mutation	p.Glu37Ter(p.E37*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SSR1

No Mutation Annotation!