Colon Cancer: Gene >> RELA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000406246
Start	65659666:65659666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406246
Start	65654584:65654584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1450G>A
AA Mutation	p.Val484Met(p.V484M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406246
Start	65662008:65662008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>A
AA Mutation	p.Glu39Lys(p.E39K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000406246
Start	65654629:65654629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405G>A
AA Mutation	p.Val469Ile(p.V469I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000406246
Start	65659667:65659667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558T>A
AA Mutation	p.Asn186Lys(p.N186K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000406246
Start	65661978:65661978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145G>A
AA Mutation	p.Glu49Lys(p.E49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406246
Start	65654756:65654756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406246
Start	65659730:65659730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534009178
CDS Mutation	c.495G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406246
Start	65654729:65654729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370929917
CDS Mutation	c.1305G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406246
Start	65654501:65654501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1533delC
AA Mutation	p.Asp512ThrfsTer35(p.D512Tfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406246
Start	65654575:65654575(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1459delC
AA Mutation	p.His487ThrfsTer7(p.H487Tfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406246
Start	65654472:65654472(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1562delC
AA Mutation	p.Pro521ArgfsTer26(p.P521Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RELA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406246
Start	65659705:65659705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Cys(p.R174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript