Colon Cancer: Gene >> EGFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55156650:55156650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124C>T
AA Mutation	p.Ala375Val(p.A375V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55201335:55201335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3094A>T
AA Mutation	p.Thr1032Ser(p.T1032S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55143409:55143409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345T>G
AA Mutation	p.Asn115Lys(p.N115K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55143465:55143465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401A>G
AA Mutation	p.Glu134Gly(p.E134G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55155847:55155847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>C
AA Mutation	p.Asp303His(p.D303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55155880:55155880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552062864
CDS Mutation	c.940G>A
AA Mutation	p.Asp314Asn(p.D314N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55152581:55152581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55201257:55201257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3016G>A
AA Mutation	p.Asp1006Asn(p.D1006N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55155866:55155866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926G>A
AA Mutation	p.Arg309Gln(p.R309Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55205271:55205271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3287C>T
AA Mutation	p.Ser1096Phe(p.S1096F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55201240:55201240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2999C>T
AA Mutation	p.Ala1000Val(p.A1000V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55205438:55205438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368892932
CDS Mutation	c.3454G>A
AA Mutation	p.Asp1152Asn(p.D1152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55192831:55192831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2691C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55156798:55156798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55198763:55198763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41396448
CDS Mutation	c.2748C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55156645:55156645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2302536
CDS Mutation	c.1119G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55154040:55154040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55142317:55142317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275493
Start	55205287:55205287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55796214
CDS Mutation	c.3303C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EGFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55174795:55174795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559717059
CDS Mutation	c.2258C>T
AA Mutation	p.Pro753Leu(p.P753L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55143404:55143404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>A
AA Mutation	p.Glu114Lys(p.E114K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275493
Start	55143444:55143444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380C>A
AA Mutation	p.Ala127Glu(p.A127E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript