Colon Cancer: Gene >> SGMS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361781
Start	50327301:50327301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645T>G
AA Mutation	p.Phe215Leu(p.F215L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361781
Start	50343505:50343505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>T
AA Mutation	p.Leu204Phe(p.L204F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361781
Start	50343649:50343649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>T
AA Mutation	p.Val156Phe(p.V156F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361781
Start	50311371:50311371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361781
Start	50343833:50343833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775055834
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361781
Start	50343644:50343644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772026516
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361781
Start	50343881:50343881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361781
Start	50343977:50343977(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.138delA
AA Mutation	p.Lys46AsnfsTer18(p.K46Nfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SGMS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361781
Start	50307224:50307224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387Gln(p.R387Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript