Colon Cancer: Gene >> HIST1H3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621411
Start	26031957:26031957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104G>A
AA Mutation	p.Gly35Asp(p.G35D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000621411
Start	26031843:26031843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218G>C
AA Mutation	p.Arg73Pro(p.R73P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000621411
Start	26031841:26031841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>C
AA Mutation	p.Glu74Gln(p.E74Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000621411
Start	26031946:26031946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115C>T
AA Mutation	p.Pro39Ser(p.P39S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000621411
Start	26031715:26031715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346A>G
AA Mutation	p.Lys116Glu(p.K116E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000621411
Start	26031948:26031948(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.113delA
AA Mutation	p.Lys38SerfsTer25(p.K38Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HIST1H3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621411
Start	26031803:26031803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>C
AA Mutation	p.Gln86His(p.Q86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript