Colon Cancer: Gene >> RUFY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70775197:70775197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788A>T
AA Mutation	p.Gln263Leu(p.Q263L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381006
Start	70804402:70804402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1705G>A
AA Mutation	p.Gly569Ser(p.G569S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70788932:70788932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198G>T
AA Mutation	p.Asp400Tyr(p.D400Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70763641:70763641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70722638:70722638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65C>T
AA Mutation	p.Ala22Val(p.A22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70722598:70722598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25G>A
AA Mutation	p.Asp9Asn(p.D9N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70783103:70783103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907A>G
AA Mutation	p.Asn303Asp(p.N303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70788841:70788841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1107G>T
AA Mutation	p.Met369Ile(p.M369I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381006
Start	70806654:70806654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1858T>G
AA Mutation	p.Ser620Ala(p.S620A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226328
Start	70768562:70768562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000226328
Start	70788920:70788920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186C>T
AA Mutation	p.Gln396Ter(p.Q396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RUFY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226328
Start	70764506:70764506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226328
Start	70762685:70762685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript