Colon Cancer: Gene >> CYTH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6164955:6164955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192A>T
AA Mutation	p.Asn398Tyr(p.N398Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6173713:6173713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389T>C
AA Mutation	p.Val130Ala(p.V130A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6165786:6165786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6190470:6190470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96G>T
AA Mutation	p.Lys32Asn(p.K32N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6170944:6170944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597G>A
AA Mutation	p.Met199Ile(p.M199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6187111:6187111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184752712
CDS Mutation	c.188C>T
AA Mutation	p.Thr63Met(p.T63M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6171278:6171278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760794383
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6165353:6165353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761402109
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6170884:6170884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396741
Start	6170902:6170902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396741
Start	6164946:6164947(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1200dupA
AA Mutation	p.Ter401IlefsTer10(p.*401Ifs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CYTH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396741
Start	6190465:6190465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101T>G
AA Mutation	p.Leu34Arg(p.L34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000396741
Start	6165428:6165428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript