Colon Cancer: Gene >> METTL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2438146:2438146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851C>T
AA Mutation	p.Ala284Val(p.A284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2420397:2420397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262A>T
AA Mutation	p.Glu421Val(p.E421V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2464337:2464337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2420864:2420864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929A>T
AA Mutation	p.Lys310Ile(p.K310I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263092
Start	2420003:2420003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263092
Start	2420785:2420785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776550789
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263092
Start	2420748:2420748(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1045delA
AA Mutation	p.Ile349PhefsTer5(p.I349Ffs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000263092
Start	2420398:2420398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261G>T
AA Mutation	p.Glu421Ter(p.E421*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263092
Start	2464214:2464215(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.721dupA
AA Mutation	p.Arg241LysfsTer6(p.R241Kfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> METTL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2420544:2420544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115C>T
AA Mutation	p.Thr372Met(p.T372M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2464337:2464337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263092
Start	2477827:2477827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>T
AA Mutation	p.Asp63Tyr(p.D63Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263092
Start	2420051:2420051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608T>C
Mutation Classification	Silent
Feature Type	Transcript