Colon Cancer: Gene >> QRSL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106654890:106654890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010C>T
AA Mutation	p.Ser337Leu(p.S337L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106652328:106652328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761098365
CDS Mutation	c.677C>T
AA Mutation	p.Ser226Leu(p.S226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106652301:106652301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650G>A
AA Mutation	p.Arg217His(p.R217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106640504:106640504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>C
AA Mutation	p.Lys60Asn(p.K60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106665857:106665857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142696796
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106663060:106663060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241G>C
AA Mutation	p.Gly414Ala(p.G414A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106649186:106649186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776695628
CDS Mutation	c.542C>T
AA Mutation	p.Ala181Val(p.A181V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369046
Start	106652549:106652549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369046
Start	106649118:106649118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369046
Start	106663103:106663103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000369046
Start	106652214:106652214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563T>A
AA Mutation	p.Leu188Ter(p.L188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> QRSL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106665916:106665916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501C>T
AA Mutation	p.Pro501Ser(p.P501S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369046
Start	106655704:106655704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132C>A
AA Mutation	p.Leu378Ile(p.L378I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369046
Start	106649046:106649046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402A>G
Mutation Classification	Silent
Feature Type	Transcript