Colon Cancer: Gene >> RFC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296273
Start	186794763:186794763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777641769
CDS Mutation	c.305G>A
AA Mutation	p.Arg102Gln(p.R102Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296273
Start	186794694:186794694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374A>C
AA Mutation	p.Asn125Thr(p.N125T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000296273
Start	186790255:186790255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>C
AA Mutation	p.Asp295His(p.D295H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296273
Start	186792933:186792933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>T
AA Mutation	p.Pro142Leu(p.P142L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296273
Start	186797605:186797605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>A
AA Mutation	p.Leu74Ile(p.L74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296273
Start	186804618:186804619(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.95dupA
AA Mutation	p.Asn32LysfsTer20(p.N32Kfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296273
Start	186789987:186789988(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1073dupA
AA Mutation	p.Leu359ValfsTer8(p.L359Vfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000296273
Start	186790256:186790256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RFC4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296273
Start	186790017:186790017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript