Colon Cancer: Gene >> ZSWIM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13830249:13830249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2169G>T
AA Mutation	p.Glu723Asp(p.E723D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13799811:13799811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245A>G
AA Mutation	p.Tyr82Cys(p.Y82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13809092:13809092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770827401
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13830397:13830397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317C>T
AA Mutation	p.Pro773Ser(p.P773S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13819423:13819423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751893324
CDS Mutation	c.1640G>A
AA Mutation	p.Arg547His(p.R547H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13817823:13817823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420G>A
AA Mutation	p.Gly474Arg(p.G474R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254323
Start	13809108:13809108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373743399
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZSWIM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13817231:13817231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196G>A
AA Mutation	p.Gly399Asp(p.G399D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13830299:13830299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2219G>A
AA Mutation	p.Arg740Gln(p.R740Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254323
Start	13817239:13817239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204T>C
AA Mutation	p.Cys402Arg(p.C402R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript