Colon Cancer: Gene >> ORAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446957:102446957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771911609
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Cys(p.R224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446559:102446559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372227034
CDS Mutation	c.272G>A
AA Mutation	p.Arg91Gln(p.R91Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446967:102446967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680C>T
AA Mutation	p.Thr227Met(p.T227M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446709:102446709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752254400
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446942:102446942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655T>C
AA Mutation	p.Tyr219His(p.Y219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446784:102446784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497T>C
AA Mutation	p.Val166Ala(p.V166A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356387
Start	102439103:102439103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374851154
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ORAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356387
Start	102446697:102446697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410C>T
AA Mutation	p.Ser137Phe(p.S137F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript