Colon Cancer: Gene >> HMGB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339872
Start	30462566:30462566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443C>G
AA Mutation	p.Ala148Gly(p.A148G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339872
Start	30461381:30461381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624A>T
AA Mutation	p.Glu208Asp(p.E208D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339872
Start	30463550:30463550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131A>C
AA Mutation	p.Lys44Thr(p.K44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339872
Start	30462631:30462631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339872
Start	30462562:30462562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753022161
CDS Mutation	c.447G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HMGB1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339872
Start	30462631:30462631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript