Colon Cancer: Gene >> GNAI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351004
Start	80211001:80211001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623G>A
AA Mutation	p.Arg208Gln(p.R208Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351004
Start	80199235:80199235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758691743
CDS Mutation	c.314G>A
AA Mutation	p.Arg105His(p.R105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351004
Start	80211037:80211037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659C>T
AA Mutation	p.Ala220Val(p.A220V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351004
Start	80212790:80212790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795A>G
AA Mutation	p.Ile265Met(p.I265M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351004
Start	80135265:80135265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000351004
Start	80211098:80211099(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.720_720+1insA
AA Mutation	p.Asn241LysfsTer5(p.N241Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GNAI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351004
Start	80211036:80211036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351004
Start	80211068:80211068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs71555062
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript