Colon Cancer: Gene >> C11orf53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280325
Start	111285864:111285864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521C>T
AA Mutation	p.Pro174Leu(p.P174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280325
Start	111284175:111284175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107C>T
AA Mutation	p.Ser36Phe(p.S36F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280325
Start	111285726:111285726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>T
AA Mutation	p.Thr128Ile(p.T128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280325
Start	111284136:111284136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68T>C
AA Mutation	p.Phe23Ser(p.F23S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280325
Start	111285980:111285980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637C>T
AA Mutation	p.His213Tyr(p.H213Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280325
Start	111284206:111284206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280325
Start	111284226:111284227(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.158_159insT
AA Mutation	p.Ala54GlyfsTer51(p.A54Gfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000280325
Start	111284075:111284075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> C11orf53

No Mutation Annotation!