Colon Cancer: Gene >> SEMG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45207685:45207685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>T
AA Mutation	p.His130Tyr(p.H130Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45207646:45207646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349G>T
AA Mutation	p.Asp117Tyr(p.D117Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45208636:45208636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339C>T
AA Mutation	p.Arg447Cys(p.R447C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45208340:45208340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043A>G
AA Mutation	p.Tyr348Cys(p.Y348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45207112:45207112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59C>T
AA Mutation	p.Ala20Val(p.A20V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45207980:45207980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683A>C
AA Mutation	p.Glu228Ala(p.E228A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372781
Start	45208458:45208458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161A>C
AA Mutation	p.Gln387His(p.Q387H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372781
Start	45208020:45208020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201859336
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SEMG1

No Mutation Annotation!