Colon Cancer: Gene >> ERCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13934287:13934287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198G>T
AA Mutation	p.Ala400Ser(p.A400S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13934267:13934267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178C>T
AA Mutation	p.Ala393Val(p.A393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13947746:13947746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2150T>C
AA Mutation	p.Ile717Thr(p.I717T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13948204:13948204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562305007
CDS Mutation	c.2608G>A
AA Mutation	p.Val870Ile(p.V870I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13935664:13935664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202186213
CDS Mutation	c.1732G>A
AA Mutation	p.Val578Met(p.V578M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13948186:13948186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587778284
CDS Mutation	c.2590C>T
AA Mutation	p.Arg864Cys(p.R864C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13928201:13928201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758C>T
AA Mutation	p.Ser253Phe(p.S253F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13928123:13928123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680C>T
AA Mutation	p.Thr227Ile(p.T227I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13947810:13947810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2214C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13944789:13944789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1971A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13948038:13948038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2442G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13935600:13935600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759296999
CDS Mutation	c.1668G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13930775:13930775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13947765:13947765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2020959
CDS Mutation	c.2169C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311895
Start	13937846:13937846(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1896delA
AA Mutation	p.Lys632AsnfsTer3(p.K632Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000311895
Start	13932201:13932201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Ter(p.R340*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ERCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13935553:13935553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>A
AA Mutation	p.Asp541Asn(p.D541N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311895
Start	13948291:13948291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2695G>C
AA Mutation	p.Asp899His(p.D899H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13935216:13935216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3136151
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311895
Start	13947903:13947903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765321722
CDS Mutation	c.2307C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000311895
Start	13930739:13930739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769764837
CDS Mutation	c.822G>A
AA Mutation	p.Trp274Ter(p.W274*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript