Colon Cancer: Gene >> SCRT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000569446
Start	144333238:144333238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994G>A
AA Mutation	p.Ala332Thr(p.A332T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000569446
Start	144333241:144333241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781866174
CDS Mutation	c.991G>A
AA Mutation	p.Gly331Ser(p.G331S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000569446
Start	144333504:144333504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728C>T
AA Mutation	p.Thr243Met(p.T243M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000569446
Start	144333395:144333395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000569446
Start	144336092:144336092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000569446
Start	144333962:144333962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000569446
Start	144333290:144333290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SCRT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000569446
Start	144333413:144333413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819G>T
AA Mutation	p.Glu273Asp(p.E273D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript