Colon Cancer: Gene >> STK38L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389032
Start	27315059:27315059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717G>T
AA Mutation	p.Lys239Asn(p.K239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389032
Start	27297828:27297828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108T>G
AA Mutation	p.Ile36Met(p.I36M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389032
Start	27308347:27308347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389032
Start	27319392:27319392(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1149delT
AA Mutation	p.Phe383LeufsTer9(p.F383Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STK38L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389032
Start	27315323:27315323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810A>C
AA Mutation	p.Glu270Asp(p.E270D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389032
Start	27315088:27315088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746A>C
AA Mutation	p.Asn249Thr(p.N249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000389032
Start	27308372:27308372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>T
AA Mutation	p.Glu74Ter(p.E74*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript