Colon Cancer: Gene >> RING1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374656
Start	33211995:33211995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748416763
CDS Mutation	c.1112C>T
AA Mutation	p.Ala371Val(p.A371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374656
Start	33212299:33212299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121C>T
AA Mutation	p.Thr374Met(p.T374M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374656
Start	33211445:33211445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>T
AA Mutation	p.Ser248Ile(p.S248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374656
Start	33208875:33208875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53T>G
AA Mutation	p.Leu18Arg(p.L18R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374656
Start	33209933:33209933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145844429
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374656
Start	33211844:33211844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.965delG
AA Mutation	p.Gly322AlafsTer54(p.G322Afs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374656
Start	33211213:33211213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs761874510
CDS Mutation	c.517delG
AA Mutation	p.Glu173LysfsTer14(p.E173Kfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374656
Start	33211437:33211437(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.740delC
AA Mutation	p.Pro247GlnfsTer38(p.P247Qfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374656
Start	33211348:33211348(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.650delG
AA Mutation	p.Gly217GlufsTer68(p.G217Efs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RING1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374656
Start	33211973:33211973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090T>C
AA Mutation	p.Tyr364His(p.Y364H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374656
Start	33210043:33210043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746185117
CDS Mutation	c.368G>A
AA Mutation	p.Arg123Gln(p.R123Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374656
Start	33209668:33209668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121T>C
AA Mutation	p.Ser41Pro(p.S41P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript