Colon Cancer: Gene >> CADM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159192622:159192622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Glu92Lys(p.E92K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159199795:159199795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997A>G
AA Mutation	p.Ile333Val(p.I333V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159199798:159199798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000G>A
AA Mutation	p.Gly334Ser(p.G334S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159197022:159197022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914T>C
AA Mutation	p.Met305Thr(p.M305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159194002:159194002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653G>A
AA Mutation	p.Gly218Glu(p.G218E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159193482:159193482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159200893:159200893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168G>T
AA Mutation	p.Gly390Trp(p.G390W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159171832:159171832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>A
AA Mutation	p.Gly23Arg(p.G23R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159196394:159196394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722C>A
AA Mutation	p.Pro241His(p.P241H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159193942:159193942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593T>G
AA Mutation	p.Val198Gly(p.V198G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159197009:159197009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901G>T
AA Mutation	p.Ala301Ser(p.A301S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159196443:159196443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373766355
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159193442:159193442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159193442:159193442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159200871:159200871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159193964:159193964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367893559
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159199797:159199797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774303512
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159193970:159193970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371655700
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CADM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159193927:159193927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578C>T
AA Mutation	p.Ser193Leu(p.S193L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159194032:159194032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683A>C
AA Mutation	p.Glu228Ala(p.E228A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368125
Start	159193461:159193461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421T>G
AA Mutation	p.Ser141Ala(p.S141A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368125
Start	159199806:159199806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767354987
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000368125
Start	159193551:159193551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>T
AA Mutation	p.Glu171Ter(p.E171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript