Colon Cancer: Gene >> LCOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96955837:96955837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763089848
CDS Mutation	c.1217C>T
AA Mutation	p.Ser406Leu(p.S406L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96949289:96949289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>A
AA Mutation	p.Glu78Lys(p.E78K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96955494:96955494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874T>G
AA Mutation	p.Leu292Val(p.L292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96955479:96955479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>A
AA Mutation	p.Ala287Thr(p.A287T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96955003:96955003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383A>C
AA Mutation	p.Asp128Ala(p.D128A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96955653:96955653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Cys(p.R345C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96949125:96949125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762257326
CDS Mutation	c.68G>A
AA Mutation	p.Ser23Asn(p.S23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356016
Start	96955604:96955604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751588970
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356016
Start	96955814:96955814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000356016
Start	96955104:96955104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>T
AA Mutation	p.Glu162Ter(p.E162*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356016
Start	96955772:96955773(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1152_1153insTGTCTGT
AA Mutation	p.Lys385CysfsTer3(p.K385Cfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356016
Start	96955909:96955910(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1295dupA
AA Mutation	p.Asn432LysfsTer7(p.N432Kfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LCOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356016
Start	96955543:96955543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923G>A
AA Mutation	p.Gly308Glu(p.G308E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript