Colon Cancer: Gene >> UQCRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268379
Start	21976176:21976176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057G>T
AA Mutation	p.Ala353Ser(p.A353S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268379
Start	21980611:21980611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189G>A
AA Mutation	p.Gly397Arg(p.G397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268379
Start	21957546:21957546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>A
AA Mutation	p.Leu83Met(p.L83M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268379
Start	21957553:21957553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254T>C
AA Mutation	p.Leu85Pro(p.L85P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268379
Start	21957292:21957292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761498645
CDS Mutation	c.91G>A
AA Mutation	p.Ala31Thr(p.A31T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268379
Start	21983147:21983147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268379
Start	21957554:21957554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_lost
Transcription ID	ENST00000268379
Start	21983169:21983169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1360T>C
AA Mutation	p.Ter454GlnextTer2(p.*454Qext*2)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UQCRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268379
Start	21957516:21957516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>C
AA Mutation	p.Asp73His(p.D73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript