Colon Cancer: Gene >> TRMT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000203001
Start	5950281:5950281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125G>A
AA Mutation	p.Arg42Lys(p.R42K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000203001
Start	5941100:5941100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255G>T
AA Mutation	p.Gly419Trp(p.G419W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000203001
Start	5943648:5943648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766405213
CDS Mutation	c.578C>T
AA Mutation	p.Thr193Met(p.T193M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000203001
Start	5943626:5943626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000203001
Start	5941959:5941959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000203001
Start	5946515:5946515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.147delA
AA Mutation	p.Lys49AsnfsTer20(p.K49Nfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000203001
Start	5944162:5944162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780358338
CDS Mutation	c.458delA
AA Mutation	p.Lys153AsnfsTer9(p.K153Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000203001
Start	5942569:5942569(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.885delA
AA Mutation	p.Lys295AsnfsTer64(p.K295Nfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000203001
Start	5944214:5944214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Ter(p.R136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRMT6

No Mutation Annotation!