Colon Cancer: Gene >> SUCLG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307227
Start	67520558:67520558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494C>T
AA Mutation	p.Pro165Leu(p.P165L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307227
Start	67495853:67495853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007G>A
AA Mutation	p.Gly336Asp(p.G336D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307227
Start	67498148:67498148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905A>C
AA Mutation	p.Asn302Thr(p.N302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307227
Start	67528171:67528171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779436281
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307227
Start	67400780:67400780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307227
Start	67520557:67520557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200035351
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SUCLG2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307227
Start	67529158:67529158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript