Colon Cancer: Gene >> FGGY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59607816:59607816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768288661
CDS Mutation	c.917C>T
AA Mutation	p.Pro306Leu(p.P306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59456975:59456975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>C
AA Mutation	p.Leu190Pro(p.L190P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59607839:59607839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940G>T
AA Mutation	p.Gly314Trp(p.G314W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59321584:59321584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35A>G
AA Mutation	p.Tyr12Cys(p.Y12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59346259:59346259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531685698
CDS Mutation	c.326G>A
AA Mutation	p.Arg109Gln(p.R109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303721
Start	59554209:59554209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116481036
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303721
Start	59674109:59674109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757211105
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000303721
Start	59339991:59339991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748040209
CDS Mutation	c.235C>T
AA Mutation	p.Arg79Ter(p.R79*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303721
Start	59346344:59346345(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759562134
CDS Mutation	c.418dupG
AA Mutation	p.Val140GlyfsTer25(p.V140Gfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGGY

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59762525:59762525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597G>A
AA Mutation	p.Val533Ile(p.V533I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303721
Start	59346382:59346382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449T>G
AA Mutation	p.Leu150Arg(p.L150R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript