Colon Cancer: Gene >> ECE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21258833:21258833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>T
AA Mutation	p.Gly208Cys(p.G208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21256065:21256065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368124166
CDS Mutation	c.902G>A
AA Mutation	p.Arg301Gln(p.R301Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21220056:21220056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142918103
CDS Mutation	c.2212C>T
AA Mutation	p.Arg738Trp(p.R738W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21258761:21258761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21225420:21225420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870G>A
AA Mutation	p.Gly624Arg(p.G624R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21225408:21225408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1882C>T
AA Mutation	p.Pro628Ser(p.P628S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21247302:21247302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082T>C
AA Mutation	p.Ile361Thr(p.I361T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21225320:21225320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1970A>G
AA Mutation	p.Glu657Gly(p.E657G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21245030:21245030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237G>A
AA Mutation	p.Ala413Thr(p.A413T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21272766:21272766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21221816:21221816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201715054
CDS Mutation	c.2067C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21247292:21247292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143000531
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21219967:21219967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752479442
CDS Mutation	c.2301C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21272757:21272757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21228014:21228014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563985263
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21227190:21227190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000374893
Start	21290158:21290158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ECE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21272852:21272852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340T>G
AA Mutation	p.Ser114Ala(p.S114A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374893
Start	21236838:21236838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750088524
CDS Mutation	c.1396G>A
AA Mutation	p.Glu466Lys(p.E466K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21228014:21228014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563985263
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374893
Start	21272889:21272889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765200448
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript