Colon Cancer: Gene >> TIPARP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156695995:156695995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771589802
CDS Mutation	c.1217G>A
AA Mutation	p.Arg406His(p.R406H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156677711:156677711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14C>G
AA Mutation	p.Thr5Ser(p.T5S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156677903:156677903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206T>G
AA Mutation	p.Leu69Arg(p.L69R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156678095:156678095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147956353
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295924
Start	156678087:156678087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295924
Start	156694125:156694128(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1025_1028delTTTA
AA Mutation	p.Ile342ThrfsTer25(p.I342Tfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000295924
Start	156678094:156678094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Ter(p.R133*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295924
Start	156705111:156705112(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1954_1955insTAAAG
AA Mutation	p.Ser652IlefsTer15(p.S652Ifs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000295924
Start	156678468:156678469(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.771_772insAAAACTGTTTTC
AA Mutation	p.Cys257_Leu258insLysThrValPhe(p.C257_L258insKTVF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TIPARP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156678295:156678295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598C>A
AA Mutation	p.Leu200Met(p.L200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156678423:156678423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726T>G
AA Mutation	p.Ile242Met(p.I242M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295924
Start	156678565:156678565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>A
AA Mutation	p.Glu290Lys(p.E290K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000295924
Start	156694027:156694027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>T
AA Mutation	p.Glu309Ter(p.E309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript