Colon Cancer: Gene >> DCLRE1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113842409:113842409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2599A>G
AA Mutation	p.Thr867Ala(p.T867A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113835184:113835184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3091T>G
AA Mutation	p.Phe1031Val(p.F1031V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113850126:113850126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200392207
CDS Mutation	c.979G>A
AA Mutation	p.Glu327Lys(p.E327K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113850495:113850495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>T
AA Mutation	p.Gly204Cys(p.G204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113845773:113845773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2290C>A
AA Mutation	p.His764Asn(p.H764N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113849389:113849389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716G>T
AA Mutation	p.Glu572Asp(p.E572D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361384
Start	113849008:113849008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2097G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361384
Start	113850157:113850157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760137335
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361384
Start	113849640:113849640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184992773
CDS Mutation	c.1465T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361384
Start	113849198:113849198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747223502
CDS Mutation	c.1907delA
AA Mutation	p.Lys636ArgfsTer31(p.K636Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361384
Start	113841535:113841535(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2691delA
AA Mutation	p.Val898TrpfsTer37(p.V898Wfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361384
Start	113850487:113850488(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.617_618insCAACAAAATCTGTAAA
AA Mutation	p.Cys207AsnfsTer7(p.C207Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DCLRE1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113852984:113852984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Leu67Phe(p.L67F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113849529:113849529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576T>G
AA Mutation	p.Leu526Val(p.L526V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361384
Start	113849939:113849939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166C>A
AA Mutation	p.Ser389Tyr(p.S389Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361384
Start	113849509:113849509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181214695
CDS Mutation	c.1596G>A
Mutation Classification	Silent
Feature Type	Transcript