Colon Cancer: Gene >> FLT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28015227:28015227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2683G>T
AA Mutation	p.Asp895Tyr(p.D895Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28023357:28023357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2411T>G
AA Mutation	p.Phe804Cys(p.F804C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28023470:28023470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2298T>G
AA Mutation	p.Ile766Met(p.I766M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28049504:28049504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746967379
CDS Mutation	c.916A>C
AA Mutation	p.Asn306His(p.N306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28049489:28049489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Trp(p.R311W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28015232:28015232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2678C>T
AA Mutation	p.Pro893Leu(p.P893L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28004077:28004077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587778369
CDS Mutation	c.2957C>T
AA Mutation	p.Pro986Leu(p.P986L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28049641:28049641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201609515
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28057407:28057407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28057408:28057408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28033918:28033918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28015630:28015630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2613C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241453
Start	28004078:28004079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2955_2956delTC
AA Mutation	p.Pro986AlafsTer27(p.P986Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000241453
Start	28033916:28033916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1913C>G
AA Mutation	p.Ser638Ter(p.S638*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000241453
Start	28052544:28052544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FLT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28027134:28027134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161C>A
AA Mutation	p.His721Asn(p.H721N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28048309:28048309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171C>T
AA Mutation	p.Pro391Ser(p.P391S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28027097:28027097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2198C>A
AA Mutation	p.Pro733Gln(p.P733Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28062022:28062022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>A
AA Mutation	p.Ser71Arg(p.S71R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241453
Start	28062023:28062023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212G>T
AA Mutation	p.Ser71Ile(p.S71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28052619:28052619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56033040
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28015597:28015597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2646C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241453
Start	28061950:28061950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371992934
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript