Mutation

Primary Site >> Stomach Cancer

Gene >> ERCC3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127272941:127272941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1751C>T
AA Mutation	p.Thr584Met(p.T584M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127289421:127289421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738G>A
AA Mutation	p.Met246Ile(p.M246I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127271347:127271347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1934G>A
AA Mutation	p.Arg645Gln(p.R645Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127293602:127293602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145T>C
AA Mutation	p.Ser49Pro(p.S49P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127257654:127257654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189511674
CDS Mutation	c.2291C>T
AA Mutation	p.Ser764Leu(p.S764L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127286808:127286808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237C>A
AA Mutation	p.Leu413Met(p.L413M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127289382:127289382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772883177
CDS Mutation	c.777A>T
AA Mutation	p.Glu259Asp(p.E259D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285398
Start	127286979:127286979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066A>G
AA Mutation	p.Thr356Ala(p.T356A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127293654:127293654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127272949:127272949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147061557
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127280570:127280570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127293627:127293627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127271358:127271358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1923G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285398
Start	127292751:127292751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285398
Start	127272930:127272930(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1762delG
AA Mutation	p.Glu588LysfsTer23(p.E588Kfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript