Colon Cancer: Gene >> ARHGDIB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14950535:14950535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.178A>G
AA Mutation	p.Thr60Ala(p.T60A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14942613:14942613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515A>G
AA Mutation	p.Tyr172Cys(p.Y172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14947892:14947892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323G>T
AA Mutation	p.Arg108Ile(p.R108I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14942698:14942698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>T
AA Mutation	p.Gly144Cys(p.G144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14947882:14947882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333T>G
AA Mutation	p.Ile111Met(p.I111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14942625:14942625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369111462
CDS Mutation	c.503C>T
AA Mutation	p.Ala168Val(p.A168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000228945
Start	14942547:14942547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774401441
CDS Mutation	c.581C>T
AA Mutation	p.Ser194Leu(p.S194L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228945
Start	14942546:14942546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748771676
CDS Mutation	c.582G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGDIB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228945
Start	14944816:14944816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript