Colon Cancer: Gene >> CHRDL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74702860:74702860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376221805
CDS Mutation	c.1054C>T
AA Mutation	p.Arg352Cys(p.R352C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74713422:74713422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>C
AA Mutation	p.Val85Leu(p.V85L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74696555:74696555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244T>C
AA Mutation	p.Leu415Pro(p.L415P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74730846:74730846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141077727
CDS Mutation	c.43G>A
AA Mutation	p.Ala15Thr(p.A15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74704566:74704566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>A
AA Mutation	p.Ser224Asn(p.S224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376332
Start	74706488:74706488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581T>C
AA Mutation	p.Val194Ala(p.V194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74702929:74702929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985A>G
AA Mutation	p.Thr329Ala(p.T329A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74702907:74702907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007G>T
AA Mutation	p.Gly336Val(p.G336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74710884:74710884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Cys(p.R133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74710944:74710944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>T
AA Mutation	p.His113Tyr(p.H113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376332
Start	74710921:74710921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748176031
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376332
Start	74706499:74706499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112976652
CDS Mutation	c.570G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376332
Start	74703428:74703428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376332
Start	74702909:74702909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146909868
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHRDL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376332
Start	74703394:74703394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141892720
CDS Mutation	c.857G>A
AA Mutation	p.Arg286His(p.R286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376332
Start	74713444:74713444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555934347
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000376332
Start	74718744:74718744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171C>A
AA Mutation	p.Tyr57Ter(p.Y57*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript