Colon Cancer: Gene >> PRMT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3550059:3550059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3592330:3592330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079T>C
AA Mutation	p.Met360Thr(p.M360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3550030:3550030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>T
AA Mutation	p.Gly119Val(p.G119V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3553654:3553654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421G>A
AA Mutation	p.Glu141Lys(p.E141K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3569519:3569519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200858548
CDS Mutation	c.667G>A
AA Mutation	p.Val223Met(p.V223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3583127:3583127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898C>T
AA Mutation	p.Arg300Cys(p.R300C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3592310:3592310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059A>C
AA Mutation	p.Glu353Asp(p.E353D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382622
Start	3583096:3583096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760968981
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382622
Start	3583144:3583144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370738399
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382622
Start	3491676:3491676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382622
Start	3576914:3576914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758189251
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382622
Start	3569518:3569518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763610227
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382622
Start	3540614:3540614(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.90delC
AA Mutation	p.Ser31ProfsTer35(p.S31Pfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRMT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382622
Start	3593177:3593177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Cys(p.R394C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000382622
Start	3593099:3593099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768625467
CDS Mutation	c.1102C>T
AA Mutation	p.Arg368Ter(p.R368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript