Colon Cancer: Gene >> PAX8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263334
Start	113235430:113235430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051G>A
AA Mutation	p.Val351Met(p.V351M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263334
Start	113242044:113242044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114736880
CDS Mutation	c.565G>A
AA Mutation	p.Ala189Thr(p.A189T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263334
Start	113236639:113236639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263334
Start	113241669:113241669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263334
Start	113242071:113242071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538T>C
AA Mutation	p.Tyr180His(p.Y180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263334
Start	113236683:113236683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263334
Start	113241709:113241709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263334
Start	113235492:113235492(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.989delT
AA Mutation	p.Leu330TrpfsTer96(p.L330Wfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000263334
Start	113227254:113227254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Ter(p.R364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PAX8

No Mutation Annotation!