Colon Cancer: Gene >> TRIM54

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27282830:27282830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>A
AA Mutation	p.Phe33Leu(p.F33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27298688:27298688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763773532
CDS Mutation	c.290G>A
AA Mutation	p.Arg97Gln(p.R97Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27306309:27306309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963A>T
AA Mutation	p.Glu321Asp(p.E321D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27299409:27299409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770394298
CDS Mutation	c.506G>A
AA Mutation	p.Arg169His(p.R169H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27298658:27298658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260T>C
AA Mutation	p.Leu87Pro(p.L87P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27306220:27306220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>A
AA Mutation	p.Ala292Thr(p.A292T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27299408:27299408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748843079
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Cys(p.R169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380075
Start	27305762:27305762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788T>G
AA Mutation	p.Leu263Arg(p.L263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380075
Start	27299251:27299251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380075
Start	27304994:27304994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000380075
Start	27298585:27298585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187C>T
AA Mutation	p.Gln63Ter(p.Q63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM54

Mutation ID	1
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000380075
Start	27305809:27305810(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.837_842dupTCTCCA
AA Mutation	p.Leu280_Gln281insHisLeu(p.L280_Q281insHL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript