Colon Cancer: Gene >> STIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	4086507:4086507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555016539
CDS Mutation	c.1505G>A
AA Mutation	p.Arg502His(p.R502H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	3967595:3967595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183G>T
AA Mutation	p.Glu61Asp(p.E61D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	4091584:4091584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145197758
CDS Mutation	c.1844G>A
AA Mutation	p.Arg615His(p.R615H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	4091668:4091668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140080199
CDS Mutation	c.1928G>A
AA Mutation	p.Arg643His(p.R643H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000300737
Start	4083498:4083498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474T>C
AA Mutation	p.Ser492Pro(p.S492P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	4082296:4082296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082A>G
AA Mutation	p.Tyr361Cys(p.Y361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300737
Start	3856348:3856348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	4074605:4074605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Trp(p.R299W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300737
Start	4082898:4082898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154A>C
AA Mutation	p.Lys385Thr(p.K385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300737
Start	4070048:4070048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201872975
CDS Mutation	c.636G>A
Mutation Classification	Silent
Feature Type	Transcript