Colon Cancer: Gene >> SRSF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373795
Start	29148486:29148486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1409C>A
AA Mutation	p.Ser470Tyr(p.S470Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373795
Start	29149099:29149099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753974067
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Cys(p.R266C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373795
Start	29159382:29159382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>C
AA Mutation	p.Asp119His(p.D119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373795
Start	29149173:29149173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368357249
CDS Mutation	c.722G>A
AA Mutation	p.Arg241Gln(p.R241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373795
Start	29148746:29148746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SRSF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373795
Start	29148546:29148546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349C>T
AA Mutation	p.Ser450Leu(p.S450L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000373795
Start	29148904:29148909(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.986_991delAGAGTC
AA Mutation	p.Gln329_Ser330del(p.Q329_S330del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript