Colon Cancer: Gene >> NFS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374092
Start	35672831:35672831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Cys(p.R412C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374092
Start	35681899:35681899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644T>A
AA Mutation	p.Ile215Asn(p.I215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374092
Start	35675169:35675169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148047173
CDS Mutation	c.824G>A
AA Mutation	p.Arg275His(p.R275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374092
Start	35680847:35680847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680T>C
AA Mutation	p.Val227Ala(p.V227A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374092
Start	35690504:35690504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470A>C
AA Mutation	p.Lys157Thr(p.K157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374092
Start	35680822:35680822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705G>T
AA Mutation	p.Gln235His(p.Q235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NFS1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374092
Start	35672842:35672842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223T>A
AA Mutation	p.Phe408Tyr(p.F408Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript