Colon Cancer: Gene >> CFHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196828149:196828149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>C
AA Mutation	p.Glu170Asp(p.E170D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196828096:196828096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>T
AA Mutation	p.Val153Leu(p.V153L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196831800:196831800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794C>T
AA Mutation	p.Pro265Leu(p.P265L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196826844:196826844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269C>A
AA Mutation	p.Pro90His(p.P90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196830503:196830503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>A
AA Mutation	p.Ser204Tyr(p.S204Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320493
Start	196825592:196825592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320493
Start	196826932:196826932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320493
Start	196826983:196826983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CFHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196830620:196830620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728T>A
AA Mutation	p.Leu243His(p.L243H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320493
Start	196830536:196830536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644A>G
AA Mutation	p.Asp215Gly(p.D215G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320493
Start	196830537:196830537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript