Colon Cancer: Gene >> BTRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370187
Start	101536604:101536604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528C>T
AA Mutation	p.Arg510Cys(p.R510C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370187
Start	101531317:101531317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824T>G
AA Mutation	p.Ile275Ser(p.I275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370187
Start	101531308:101531308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815A>G
AA Mutation	p.Tyr272Cys(p.Y272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370187
Start	101526166:101526166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>T
AA Mutation	p.Ser237Phe(p.S237F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370187
Start	101535380:101535380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374T>G
AA Mutation	p.Phe458Leu(p.F458L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370187
Start	101532416:101532416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Arg321Gln(p.R321Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370187
Start	101531303:101531303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370187
Start	101536642:101536642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1566G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370187
Start	101531270:101531270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371692654
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370187
Start	101550816:101550816(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1780delC
AA Mutation	p.Arg594ValfsTer14(p.R594Vfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BTRC

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370187
Start	101526015:101526015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Trp(p.R187W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000370187
Start	101550720:101550720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375317445
CDS Mutation	c.1678C>T
AA Mutation	p.Arg560Ter(p.R560*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript