Colon Cancer: Gene >> WT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32389137:32389137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1475A>G
AA Mutation	p.Lys492Arg(p.K492R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32392019:32392019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385G>A
AA Mutation	p.Arg462Gln(p.R462Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32392028:32392028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376A>C
AA Mutation	p.Lys459Thr(p.K459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32392052:32392052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352T>A
AA Mutation	p.Phe451Tyr(p.F451Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32396304:32396304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401Lys(p.R401K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332351
Start	32428555:32428555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332351
Start	32389064:32389064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202118284
CDS Mutation	c.1548G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332351
Start	32428603:32428603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000332351
Start	32392756:32392756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32434810:32434810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>T
AA Mutation	p.Pro179Leu(p.P179L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332351
Start	32400024:32400024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1022G>A
AA Mutation	p.Ser341Asn(p.S341N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332351
Start	32389064:32389064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202118284
CDS Mutation	c.1548G>A
Mutation Classification	Silent
Feature Type	Transcript