Colon Cancer: Gene >> FMOD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203347451:203347451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200924838
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Trp(p.R274W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203342429:203342429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Cys(p.R349C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203347300:203347300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971G>T
AA Mutation	p.Arg324Met(p.R324M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203347973:203347973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>A
AA Mutation	p.Leu100Met(p.L100M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203348063:203348063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208C>T
AA Mutation	p.Pro70Ser(p.P70S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203347955:203347955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376310218
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354955
Start	203347890:203347890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354955
Start	203348091:203348091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354955
Start	203347342:203347342(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.929delC
AA Mutation	p.Pro310GlnfsTer31(p.P310Qfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354955
Start	203347472:203347472(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.799delG
AA Mutation	p.Ala267ArgfsTer14(p.A267Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FMOD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203342429:203342429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Cys(p.R349C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203347988:203347988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768009921
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Cys(p.R95C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354955
Start	203342428:203342428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046G>A
AA Mutation	p.Arg349His(p.R349H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354955
Start	203347503:203347503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768C>A
Mutation Classification	Silent
Feature Type	Transcript