Colon Cancer: Gene >> LDHC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280704
Start	18434824:18434824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503C>G
AA Mutation	p.Ala168Gly(p.A168G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280704
Start	18451018:18451018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760395380
CDS Mutation	c.890G>A
AA Mutation	p.Arg297Gln(p.R297Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280704
Start	18446305:18446305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806G>A
AA Mutation	p.Arg269Lys(p.R269K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280704
Start	18438595:18438595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368187321
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280704
Start	18446297:18446297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000280704
Start	18446316:18446317(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.817_818insAGAAAACATAATA
AA Mutation	p.Val273GlufsTer4(p.V273Efs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LDHC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280704
Start	18415270:18415270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213C>A
AA Mutation	p.Phe71Leu(p.F71L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript