Colon Cancer: Gene >> SQSTM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389805
Start	179824207:179824207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778537429
CDS Mutation	c.557G>A
AA Mutation	p.Arg186Gln(p.R186Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389805
Start	179824037:179824037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758625124
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Trp(p.R161W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389805
Start	179833127:179833127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850T>G
AA Mutation	p.Ser284Ala(p.S284A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389805
Start	179836448:179836448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200551825
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393Gln(p.R393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389805
Start	179836542:179836542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374985304
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SQSTM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389805
Start	179836547:179836547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201239306
CDS Mutation	c.1277C>T
AA Mutation	p.Ala426Val(p.A426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389805
Start	179823876:179823876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320G>A
AA Mutation	p.Arg107Gln(p.R107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript