Colon Cancer: Gene >> ASCL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342331
Start	107775226:107775226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11C>T
AA Mutation	p.Thr4Met(p.T4M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342331
Start	107775229:107775229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342331
Start	107775651:107775651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Cys(p.R146C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342331
Start	107775254:107775254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565285072
CDS Mutation	c.39G>T
AA Mutation	p.Leu13Phe(p.L13F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342331
Start	107775227:107775227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342331
Start	107775368:107775368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342331
Start	107775320:107775320(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.109delC
AA Mutation	p.Leu37SerfsTer53(p.L37Sfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ASCL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342331
Start	107775313:107775313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98G>A
AA Mutation	p.Arg33Gln(p.R33Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript