Colon Cancer: Gene >> WNT7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13819269:13819269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773943599
CDS Mutation	c.725G>A
AA Mutation	p.Arg242His(p.R242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13875066:13875066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179T>C
AA Mutation	p.Ile60Thr(p.I60T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13819117:13819117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774758917
CDS Mutation	c.877G>A
AA Mutation	p.Ala293Thr(p.A293T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13854788:13854788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>A
AA Mutation	p.Ala105Glu(p.A105E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13875004:13875004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Cys(p.R81C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13875145:13875145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373890513
CDS Mutation	c.100G>A
AA Mutation	p.Ala34Thr(p.A34T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13819294:13819294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>A
AA Mutation	p.Glu234Lys(p.E234K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13819239:13819239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755T>C
AA Mutation	p.Leu252Pro(p.L252P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13875064:13875064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>C
AA Mutation	p.Val61Leu(p.V61L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285018
Start	13819319:13819319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285018
Start	13819172:13819172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285018
Start	13854547:13854547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149363953
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285018
Start	13818986:13818986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WNT7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285018
Start	13875076:13875076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139790545
CDS Mutation	c.169G>A
AA Mutation	p.Asp57Asn(p.D57N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285018
Start	13819172:13819172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript