Colon Cancer: Gene >> ERCC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45353133:45353133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781C>A
AA Mutation	p.Ala594Asp(p.A594D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45355718:45355718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757432268
CDS Mutation	c.1490G>A
AA Mutation	p.Arg497His(p.R497H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45364489:45364489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653C>T
AA Mutation	p.Ala218Val(p.A218V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45352226:45352226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173G>A
AA Mutation	p.Ala725Thr(p.A725T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45368727:45368727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777095373
CDS Mutation	c.263G>A
AA Mutation	p.Arg88Gln(p.R88Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45352631:45352631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769085031
CDS Mutation	c.1921C>T
AA Mutation	p.Arg641Trp(p.R641W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45357365:45357365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384T>C
AA Mutation	p.Ser462Pro(p.S462P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45361598:45361598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163T>C
AA Mutation	p.Ile388Thr(p.I388T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000391945
Start	45355676:45355676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772572683
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511Gln(p.R511Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391945
Start	45357671:45357671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142702501
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391945
Start	45361594:45361594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765430756
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391945
Start	45357650:45357650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000391945
Start	45370168:45370170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.68_70delCCT
AA Mutation	p.Ser23del(p.S23del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ERCC2

No Mutation Annotation!