Colon Cancer: Gene >> FERMT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64223085:64223085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756707894
CDS Mutation	c.1720G>A
AA Mutation	p.Ala574Thr(p.A574T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64210721:64210721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>A
AA Mutation	p.Leu91Ile(p.L91I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64223379:64223379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891G>A
AA Mutation	p.Val631Ile(p.V631I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64219974:64219974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542624473
CDS Mutation	c.1175A>G
AA Mutation	p.Asp392Gly(p.D392G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64211376:64211376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201973872
CDS Mutation	c.616G>A
AA Mutation	p.Asp206Asn(p.D206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000279227
Start	64210613:64210613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163C>T
AA Mutation	p.Arg55Cys(p.R55C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279227
Start	64223418:64223418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1930C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279227
Start	64211732:64211732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368973559
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000279227
Start	64220634:64220635(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1528dupC
AA Mutation	p.Arg510ProfsTer105(p.R510Pfs*105)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FERMT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64219920:64219920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64221026:64221026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568G>A
AA Mutation	p.Arg523Gln(p.R523Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64223413:64223413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1925C>T
AA Mutation	p.Ser642Leu(p.S642L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279227
Start	64211733:64211733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772G>T
AA Mutation	p.Asp258Tyr(p.D258Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript