Colon Cancer: Gene >> STOML1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541638
Start	73988751:73988751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541638
Start	73985345:73985345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763G>A
AA Mutation	p.Ala255Thr(p.A255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000541638
Start	73992103:73992103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121G>T
AA Mutation	p.Gly41Trp(p.G41W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000541638
Start	73985468:73985468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>A
AA Mutation	p.Arg214Ser(p.R214S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000541638
Start	73985360:73985360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748A>C
AA Mutation	p.Ser250Arg(p.S250R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541638
Start	73988764:73988764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000541638
Start	73984020:73984020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769286917
CDS Mutation	c.1114delG
AA Mutation	p.Ala372ProfsTer3(p.A372Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STOML1

No Mutation Annotation!