Colon Cancer: Gene >> RIPK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24339545:24339545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24337136:24337136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1225C>T
AA Mutation	p.Pro409Ser(p.P409S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24337456:24337456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905A>G
AA Mutation	p.Lys302Arg(p.K302R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24337395:24337395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966A>C
AA Mutation	p.Gln322His(p.Q322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24338516:24338516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>T
AA Mutation	p.Gly175Trp(p.G175W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24337189:24337189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172C>T
AA Mutation	p.Ser391Leu(p.S391L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216274
Start	24336259:24336259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216274
Start	24336904:24336904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200066851
CDS Mutation	c.1317G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216274
Start	24339177:24339177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753939778
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RIPK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216274
Start	24338014:24338014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764304131
CDS Mutation	c.691G>A
AA Mutation	p.Glu231Lys(p.E231K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216274
Start	24338292:24338292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373410782
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216274
Start	24338432:24338433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.606_607delTG
AA Mutation	p.Ser202ArgfsTer19(p.S202Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000216274
Start	24337229:24337229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132C>T
AA Mutation	p.Gln378Ter(p.Q378*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript