Colon Cancer: Gene >> WNT3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228059045:228059045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639G>T
AA Mutation	p.Glu213Asp(p.E213D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228022678:228022678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83T>C
AA Mutation	p.Val28Ala(p.V28A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228050668:228050668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752609956
CDS Mutation	c.326C>T
AA Mutation	p.Ser109Leu(p.S109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000284523
Start	228022669:228022669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745831522
CDS Mutation	c.74C>T
AA Mutation	p.Ser25Leu(p.S25L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228022710:228022710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755569705
CDS Mutation	c.115C>T
AA Mutation	p.Pro39Ser(p.P39S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228022807:228022807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212A>G
AA Mutation	p.Lys71Arg(p.K71R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228059025:228059025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Gly207Arg(p.G207R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284523
Start	228022895:228022895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767871879
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284523
Start	228059213:228059213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284523
Start	228059111:228059111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WNT3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284523
Start	228050811:228050811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778326387
CDS Mutation	c.469G>A
AA Mutation	p.Glu157Lys(p.E157K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript