Colon Cancer: Gene >> LDB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000425280
Start	102109965:102109965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Trp(p.R202W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000425280
Start	102109049:102109049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768693158
CDS Mutation	c.985G>A
AA Mutation	p.Ala329Thr(p.A329T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000425280
Start	102110930:102110930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291C>A
AA Mutation	p.Phe97Leu(p.F97L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000425280
Start	102108112:102108112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217C>T
AA Mutation	p.Thr406Met(p.T406M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000425280
Start	102108272:102108272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751950349
CDS Mutation	c.1057G>A
AA Mutation	p.Glu353Lys(p.E353K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425280
Start	102108210:102108210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771823736
CDS Mutation	c.1119C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000425280
Start	102109941:102109941(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.628delC
AA Mutation	p.Arg210AlafsTer38(p.R210Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LDB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000425280
Start	102109484:102109484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756G>A
AA Mutation	p.Met252Ile(p.M252I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425280
Start	102111487:102111487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000425280
Start	102109953:102109953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616G>T
AA Mutation	p.Glu206Ter(p.E206*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript