Colon Cancer: Gene >> FGFRL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264748
Start	1024361:1024361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769A>G
AA Mutation	p.Thr257Ala(p.T257A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264748
Start	1024925:1024925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093C>T
AA Mutation	p.Pro365Ser(p.P365S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264748
Start	1025058:1025058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759910460
CDS Mutation	c.1226C>T
AA Mutation	p.Ala409Val(p.A409V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264748
Start	1023876:1023876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493G>T
AA Mutation	p.Gly165Cys(p.G165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264748
Start	1024592:1024592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000G>T
AA Mutation	p.Gly334Cys(p.G334C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264748
Start	1025191:1025191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373825808
CDS Mutation	c.1359G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264748
Start	1022441:1022441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754122283
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264748
Start	1024966:1024966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111246053
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264748
Start	1022346:1022347(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.226_238dupCGCTTCCGCGTGC
AA Mutation	p.Leu80ProfsTer44(p.L80Pfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGFRL1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264748
Start	1023643:1023643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>T
AA Mutation	p.Asp119Tyr(p.D119Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264748
Start	1024975:1024975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146112374
CDS Mutation	c.1143C>T
Mutation Classification	Silent
Feature Type	Transcript