Colon Cancer: Gene >> RNF168

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196475257:196475257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>C
AA Mutation	p.Glu246Gln(p.E246Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196471850:196471850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1685T>G
AA Mutation	p.Val562Gly(p.V562G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196502965:196502965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209C>A
AA Mutation	p.Ser70Tyr(p.S70Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196488662:196488662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766545137
CDS Mutation	c.323G>A
AA Mutation	p.Arg108His(p.R108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196488649:196488649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336A>C
AA Mutation	p.Lys112Asn(p.K112N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196502993:196502993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181T>C
AA Mutation	p.Trp61Arg(p.W61R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196472597:196472597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938A>G
AA Mutation	p.Asn313Ser(p.N313S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318037
Start	196487456:196487456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746133414
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318037
Start	196472515:196472515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779329211
CDS Mutation	c.1020G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318037
Start	196483820:196483820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318037
Start	196503042:196503045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.129_132delCGTC
AA Mutation	p.Val44LysfsTer35(p.V44Kfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318037
Start	196472011:196472012(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1523dupC
AA Mutation	p.Thr509AsnfsTer11(p.T509Nfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000318037
Start	196472668:196472669(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.866_867insCATAAC
AA Mutation	p.Gly289_Ala290insIleThr(p.G289_A290insIT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNF168

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196472197:196472197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338C>G
AA Mutation	p.Asp446Glu(p.D446E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318037
Start	196503125:196503125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Gly17Arg(p.G17R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript