Colon Cancer: Gene >> TP53RK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372114
Start	46686788:46686788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553547069
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Cys(p.R243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372114
Start	46687046:46687046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Asp157Asn(p.D157N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372114
Start	46686846:46686846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669G>T
AA Mutation	p.Lys223Asn(p.K223N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372114
Start	46686816:46686816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372114
Start	46686995:46686995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.520delC
AA Mutation	p.Leu174TrpfsTer4(p.L174Wfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000372114
Start	46687061:46687061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Ter(p.R152*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TP53RK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372114
Start	46687060:46687060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149404267
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Gln(p.R152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript