Colon Cancer: Gene >> LMBRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69699062:69699062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319G>T
AA Mutation	p.Ser440Ile(p.S440I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69713760:69713760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140874824
CDS Mutation	c.800G>A
AA Mutation	p.Arg267His(p.R267H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69790399:69790399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143T>C
AA Mutation	p.Ile48Thr(p.I48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69741839:69741839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512C>G
AA Mutation	p.Ser171Cys(p.S171C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69796871:69796871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11C>G
AA Mutation	p.Ser4Cys(p.S4C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69699117:69699117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264C>A
AA Mutation	p.Leu422Ile(p.L422I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69719018:69719018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200207509
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Cys(p.R234C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69718985:69718985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733G>C
AA Mutation	p.Glu245Gln(p.E245Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69713724:69713724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836T>G
AA Mutation	p.Leu279Arg(p.L279R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69713655:69713655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142962811
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69700796:69700796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772350306
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370577
Start	69749400:69749400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757074437
CDS Mutation	c.414A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LMBRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69701489:69701489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>A
AA Mutation	p.Ala346Asp(p.A346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69700864:69700864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1089C>G
AA Mutation	p.Phe363Leu(p.F363L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69700809:69700809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561540830
CDS Mutation	c.1144A>G
AA Mutation	p.Met382Val(p.M382V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370577
Start	69676199:69676199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753073697
CDS Mutation	c.1582T>G
AA Mutation	p.Ser528Ala(p.S528A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370577
Start	69701458:69701458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000370577
Start	69700797:69700797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Ter(p.R386*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript