Colon Cancer: Gene >> CADM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115214752:115214752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>A
AA Mutation	p.Asp284Asn(p.D284N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115229265:115229265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758008656
CDS Mutation	c.569C>T
AA Mutation	p.Ser190Leu(p.S190L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115504331:115504331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64C>T
AA Mutation	p.Pro22Ser(p.P22S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115504297:115504297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98T>C
AA Mutation	p.Phe33Ser(p.F33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115178676:115178676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178T>C
AA Mutation	p.Ile393Thr(p.I393T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115231481:115231481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768807528
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115231426:115231426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489A>C
AA Mutation	p.Glu163Asp(p.E163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115240358:115240358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187A>C
AA Mutation	p.Ser63Arg(p.S63R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115231448:115231448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201626870
CDS Mutation	c.467C>T
AA Mutation	p.Ala156Val(p.A156V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115214667:115214667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115176545:115176545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>A
AA Mutation	p.Ala420Thr(p.A420T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115231467:115231467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754556437
CDS Mutation	c.448G>A
AA Mutation	p.Asp150Asn(p.D150N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115240369:115240369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176T>C
AA Mutation	p.Val59Ala(p.V59A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115178708:115178708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199720777
CDS Mutation	c.1146G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115209623:115209623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115229221:115229221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115178696:115178696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763032683
CDS Mutation	c.1158C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115176555:115176555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750612978
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115229147:115229147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CADM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000452722
Start	115240410:115240410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135G>T
AA Mutation	p.Gln45His(p.Q45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452722
Start	115178714:115178714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757194461
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript