Colon Cancer: Gene >> SRL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4192785:4192785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790A>G
AA Mutation	p.Met264Val(p.M264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4204545:4204545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>A
AA Mutation	p.Asp51Asn(p.D51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4195678:4195678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485T>C
AA Mutation	p.Leu162Pro(p.L162P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4192247:4192247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328T>C
AA Mutation	p.Leu443Pro(p.L443P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4192574:4192574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776865624
CDS Mutation	c.1001G>A
AA Mutation	p.Arg334His(p.R334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4204581:4204581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>A
AA Mutation	p.Glu39Lys(p.E39K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4192185:4192185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200610272
CDS Mutation	c.1390G>A
AA Mutation	p.Glu464Lys(p.E464K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4195582:4195582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581T>G
AA Mutation	p.Ile194Ser(p.I194S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399609
Start	4195693:4195693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775040662
CDS Mutation	c.470G>A
AA Mutation	p.Arg157His(p.R157H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399609
Start	4197872:4197872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368659942
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399609
Start	4192237:4192237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201140750
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000399609
Start	4204595:4204597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.99_101delGGA
AA Mutation	p.Arg33_Asp34delinsSer(p.R33_D34delinsS)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SRL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399609
Start	4204627:4204627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369887184
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript