Colon Cancer: Gene >> CYGB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293230
Start	76531558:76531558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369705030
CDS Mutation	c.277G>A
AA Mutation	p.Val93Met(p.V93M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293230
Start	76531055:76531055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463C>T
AA Mutation	p.Arg155Cys(p.R155C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293230
Start	76528606:76528606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749452700
CDS Mutation	c.545C>T
AA Mutation	p.Pro182Leu(p.P182L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293230
Start	76537509:76537509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Cys(p.R12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000293230
Start	76537400:76537400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143G>T
AA Mutation	p.Arg48Met(p.R48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293230
Start	76537465:76537465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78G>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYGB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293230
Start	76531600:76531600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373180768
CDS Mutation	c.235C>T
AA Mutation	p.Arg79Trp(p.R79W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript