Colon Cancer: Gene >> CXADR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284878
Start	17561434:17561434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778453029
CDS Mutation	c.791G>A
AA Mutation	p.Arg264His(p.R264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284878
Start	17547114:17547114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374465561
CDS Mutation	c.131C>T
AA Mutation	p.Thr44Met(p.T44M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284878
Start	17565517:17565517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923C>T
AA Mutation	p.Ser308Phe(p.S308F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284878
Start	17561391:17561391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284878
Start	17560727:17560727(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.602delA
AA Mutation	p.Asn201MetfsTer27(p.N201Mfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000284878
Start	17547188:17547188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205C>T
AA Mutation	p.Gln69Ter(p.Q69*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000284878
Start	17551748:17551748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CXADR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284878
Start	17565685:17565685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091T>C
AA Mutation	p.Ile364Thr(p.I364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284878
Start	17551827:17551827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>T
AA Mutation	p.Asp97Tyr(p.D97Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284878
Start	17551926:17551926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772476067
CDS Mutation	c.388A>G
AA Mutation	p.Asn130Asp(p.N130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript