Colon Cancer: Gene >> CFHR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367425
Start	196779910:196779910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>A
AA Mutation	p.Ala123Thr(p.A123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367425
Start	196788261:196788261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476C>A
AA Mutation	p.Ser159Tyr(p.S159Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367425
Start	196779911:196779911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368C>T
AA Mutation	p.Ala123Val(p.A123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367425
Start	196793400:196793400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880A>G
AA Mutation	p.Thr294Ala(p.T294A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367425
Start	196779848:196779848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>T
AA Mutation	p.Arg102Ile(p.R102I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367425
Start	196793507:196793507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368923425
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000367425
Start	196793337:196793337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>T
AA Mutation	p.Glu273Ter(p.E273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000367425
Start	196788225:196788225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440C>G
AA Mutation	p.Ser147Ter(p.S147*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CFHR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367425
Start	196788375:196788375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590G>C
AA Mutation	p.Trp197Ser(p.W197S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript