Colon Cancer: Gene >> RTKN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74426308:74426308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1627T>A
AA Mutation	p.Ser543Thr(p.S543T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000272430
Start	74441706:74441706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111G>T
AA Mutation	p.Glu37Asp(p.E37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74432584:74432584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74426551:74426551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765799493
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272430
Start	74430359:74430359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272430
Start	74428720:74428720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272430
Start	74426358:74426358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1577delC
AA Mutation	p.Pro526GlnfsTer129(p.P526Qfs*129)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272430
Start	74426393:74426393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1542delG
AA Mutation	p.Arg515AspfsTer140(p.R515Dfs*140)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272430
Start	74426322:74426323(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1612dupC
AA Mutation	p.Leu538ProfsTer42(p.L538Pfs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272430
Start	74426403:74426404(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1531dupC
AA Mutation	p.Leu511ProfsTer21(p.L511Pfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RTKN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74426443:74426443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Pro498Ser(p.P498S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74429861:74429861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722G>A
AA Mutation	p.Ser241Asn(p.S241N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74428699:74428699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889T>C
AA Mutation	p.Cys297Arg(p.C297R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272430
Start	74428851:74428851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>A
AA Mutation	p.His283Asn(p.H283N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript