Colon Cancer: Gene >> DVL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1339433:1339433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061C>T
AA Mutation	p.Pro354Leu(p.P354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1349049:1349049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17T>A
AA Mutation	p.Ile6Asn(p.I6N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1340090:1340090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376597258
CDS Mutation	c.857G>A
AA Mutation	p.Gly286Asp(p.G286D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1342702:1342702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750153032
CDS Mutation	c.227G>A
AA Mutation	p.Arg76His(p.R76H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1338537:1338537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766432002
CDS Mutation	c.1324G>A
AA Mutation	p.Ala442Thr(p.A442T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1339332:1339332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141570756
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Cys(p.R388C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1339364:1339364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130A>G
AA Mutation	p.Tyr377Cys(p.Y377C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1341677:1341677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595A>G
AA Mutation	p.Ser199Gly(p.S199G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378888
Start	1340089:1340089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142495951
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378888
Start	1338637:1338637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774744891
CDS Mutation	c.1224G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378888
Start	1336445:1336445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747313105
CDS Mutation	c.1785G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378888
Start	1340257:1340257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1140338
CDS Mutation	c.759G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378888
Start	1338119:1338119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531247891
CDS Mutation	c.1572G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000378888
Start	1336423:1336423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1807G>T
AA Mutation	p.Glu603Ter(p.E603*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DVL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1336459:1336459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1771G>A
AA Mutation	p.Glu591Lys(p.E591K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1339331:1339331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163G>A
AA Mutation	p.Arg388His(p.R388H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378888
Start	1338373:1338373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766540058
CDS Mutation	c.1403G>A
AA Mutation	p.Arg468Gln(p.R468Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378888
Start	1338529:1338529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750379091
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript