Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRMT10C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101565368:101565368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587C>T
AA Mutation	p.Ala196Val(p.A196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101565668:101565668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887A>G
AA Mutation	p.Asn296Ser(p.N296S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101565184:101565184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403T>G
AA Mutation	p.Tyr135Asp(p.Y135D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101565500:101565500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.719C>A
AA Mutation	p.Pro240His(p.P240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101565323:101565323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542G>A
AA Mutation	p.Arg181Gln(p.R181Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309922
Start	101565316:101565316(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.539delT
AA Mutation	p.Leu180TyrfsTer10(p.L180Yfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRMT10C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101565803:101565803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022A>G
AA Mutation	p.Tyr341Cys(p.Y341C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309922
Start	101564870:101564870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89G>T
AA Mutation	p.Arg30Ile(p.R30I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309922
Start	101565195:101565195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373862967
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript