Colon Cancer: Gene >> PRMT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107056875:107056875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>A
AA Mutation	p.Val54Ile(p.V54I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107057058:107057058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107057451:107057451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>A
AA Mutation	p.Val246Met(p.V246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107057795:107057795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080A>C
AA Mutation	p.Lys360Asn(p.K360N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107056858:107056858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751008530
CDS Mutation	c.143A>G
AA Mutation	p.Tyr48Cys(p.Y48C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107057735:107057735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107057258:107057258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377462998
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107057678:107057678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107057156:107057156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107057276:107057276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107056754:107056754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370078
Start	107056748:107056748(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.38delG
AA Mutation	p.Gly13AlafsTer48(p.G13Afs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000370078
Start	107057712:107057712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>T
AA Mutation	p.Gln333Ter(p.Q333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRMT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107056876:107056876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161T>C
AA Mutation	p.Val54Ala(p.V54A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370078
Start	107056962:107056962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247G>T
AA Mutation	p.Gly83Cys(p.G83C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370078
Start	107056913:107056913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript