Colon Cancer: Gene >> STIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27002959:27002959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836T>C
AA Mutation	p.Val279Ala(p.V279A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27017767:27017767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761245104
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Cys(p.R516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27017884:27017884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663C>T
AA Mutation	p.Pro555Ser(p.P555S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27017945:27017945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1724A>T
AA Mutation	p.Glu575Val(p.E575V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27017936:27017936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715G>A
AA Mutation	p.Arg572Gln(p.R572Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27022674:27022674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377370453
CDS Mutation	c.1919C>T
AA Mutation	p.Ser640Leu(p.S640L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27008865:27008865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352T>C
AA Mutation	p.Leu451Pro(p.L451P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467087
Start	27022702:27022702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467087
Start	27022621:27022621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757441641
CDS Mutation	c.1866G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467087
Start	27022924:27022924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2169C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467087
Start	27007667:27007667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762749446
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000467087
Start	27017825:27017825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1609delC
AA Mutation	p.His537ThrfsTer64(p.H537Tfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000467087
Start	27008508:27008508(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1231delC
AA Mutation	p.His411ThrfsTer13(p.H411Tfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000467087
Start	27002318:27002318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>T
AA Mutation	p.Glu243Ter(p.E243*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000467087
Start	27007563:27007563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012G>T
AA Mutation	p.Glu338Ter(p.E338*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000467087
Start	27022958:27022959(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2203_2204insTGTA
AA Mutation	p.Ser735LeufsTer9(p.S735Lfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> STIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27008802:27008802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289G>A
AA Mutation	p.Arg430Gln(p.R430Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	26919582:26919582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230A>C
AA Mutation	p.Lys77Thr(p.K77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	26957639:26957639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310G>T
AA Mutation	p.Asp104Tyr(p.D104Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27007557:27007557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Glu336Lys(p.E336K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000467087
Start	27017936:27017936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715G>A
AA Mutation	p.Arg572Gln(p.R572Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript