Colon Cancer: Gene >> CLPTM1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320895
Start	1320650:1320650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498G>A
AA Mutation	p.Asp500Asn(p.D500N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320895
Start	1320671:1320671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745665981
CDS Mutation	c.1477C>T
AA Mutation	p.Arg493Trp(p.R493W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320895
Start	1318391:1318391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770025461
CDS Mutation	c.1595C>T
AA Mutation	p.Thr532Met(p.T532M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320895
Start	1338872:1338872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764191088
CDS Mutation	c.587G>A
AA Mutation	p.Arg196Gln(p.R196Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320895
Start	1322884:1322884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202096751
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320895
Start	1337966:1337966(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.616delA
AA Mutation	p.Thr206ProfsTer17(p.T206Pfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CLPTM1L

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320895
Start	1334301:1334301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript