Colon Cancer: Gene >> MRPL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264995
Start	131490060:131490060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489A>T
AA Mutation	p.Glu163Asp(p.E163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264995
Start	131498181:131498181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377532148
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Cys(p.R156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264995
Start	131502758:131502758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64C>A
AA Mutation	p.Leu22Met(p.L22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264995
Start	131500457:131500457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264995
Start	131490036:131490036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541190683
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264995
Start	131490033:131490033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765556142
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000264995
Start	131487681:131487681(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.628delA
AA Mutation	p.Thr210LeufsTer10(p.T210Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MRPL3

No Mutation Annotation!