Colon Cancer: Gene >> FANCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35074209:35074209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1768C>A
AA Mutation	p.Pro590Thr(p.P590T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35076448:35076448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060T>C
AA Mutation	p.Cys354Arg(p.C354R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35076794:35076794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854A>G
AA Mutation	p.Glu285Gly(p.E285G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35076010:35076010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095G>T
AA Mutation	p.Glu365Asp(p.E365D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35075017:35075017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199833626
CDS Mutation	c.1546G>A
AA Mutation	p.Ala516Thr(p.A516T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35077302:35077302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776489249
CDS Mutation	c.608T>C
AA Mutation	p.Leu203Ser(p.L203S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378643
Start	35074120:35074120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378643
Start	35075295:35075295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000378643
Start	35074495:35074495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FANCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378643
Start	35074140:35074140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761695914
CDS Mutation	c.1837C>T
AA Mutation	p.Arg613Trp(p.R613W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000378643
Start	35075285:35075285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1474G>T
AA Mutation	p.Glu492Ter(p.E492*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript