Colon Cancer: Gene >> DCLRE1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378278
Start	14923033:14923033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768393244
CDS Mutation	c.1009G>A
AA Mutation	p.Ala337Thr(p.A337T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378278
Start	14919761:14919761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133C>T
AA Mutation	p.Ala378Val(p.A378V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378278
Start	14932867:14932867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767G>A
AA Mutation	p.Cys256Tyr(p.C256Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378278
Start	14908436:14908436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2051A>C
AA Mutation	p.Lys684Thr(p.K684T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000378278
Start	14934520:14934520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538G>A
AA Mutation	p.Glu180Lys(p.E180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378278
Start	14909092:14909092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378278
Start	14908434:14908434(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2053delA
AA Mutation	p.Arg685GlufsTer6(p.R685Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000378278
Start	14908590:14908590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897G>T
AA Mutation	p.Glu633Ter(p.E633*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000378278
Start	14935462:14935462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DCLRE1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378278
Start	14954007:14954007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4A>C
AA Mutation	p.Ser2Arg(p.S2R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378278
Start	14922986:14922986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765407675
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript