Colon Cancer: Gene >> ORAI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616379
Start	121641540:121641540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616379
Start	121641147:121641147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368310115
CDS Mutation	c.410C>T
AA Mutation	p.Ala137Val(p.A137V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616379
Start	121641353:121641353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616C>T
AA Mutation	p.Pro206Ser(p.P206S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000616379
Start	121641236:121641236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782538669
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Cys(p.R167C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000616379
Start	121641407:121641407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670G>A
AA Mutation	p.Val224Ile(p.V224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000616379
Start	121641562:121641562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825G>T
AA Mutation	p.Glu275Asp(p.E275D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616379
Start	121641427:121641427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616379
Start	121641625:121641625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ORAI1

No Mutation Annotation!