Colon Cancer: Gene >> SLC10A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103049438:103049438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145541774
CDS Mutation	c.770C>T
AA Mutation	p.Thr257Met(p.T257M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103051387:103051387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758416592
CDS Mutation	c.631G>A
AA Mutation	p.Val211Ile(p.V211I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103066239:103066239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200273975
CDS Mutation	c.11C>T
AA Mutation	p.Pro4Leu(p.P4L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103066027:103066027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223C>A
AA Mutation	p.Gln75Lys(p.Q75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103058324:103058324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>A
AA Mutation	p.Leu146Ile(p.L146I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103066098:103066098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152G>A
AA Mutation	p.Cys51Tyr(p.C51Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000245312
Start	103058264:103058264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>T
AA Mutation	p.Gly166Cys(p.G166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103046183:103046183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997G>A
AA Mutation	p.Glu333Lys(p.E333K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103066005:103066005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>T
AA Mutation	p.Thr82Ile(p.T82I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103066207:103066207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43T>G
AA Mutation	p.Ser15Ala(p.S15A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103051284:103051284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734C>T
AA Mutation	p.Ala245Val(p.A245V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245312
Start	103046229:103046229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245312
Start	103065887:103065887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143992162
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245312
Start	103065893:103065893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201634783
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245312
Start	103049305:103049305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199679714
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245312
Start	103065980:103065980(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.270delT
AA Mutation	p.Phe90LeufsTer9(p.F90Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC10A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103049443:103049443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>G
AA Mutation	p.Cys255Trp(p.C255W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103049313:103049313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200823529
CDS Mutation	c.895G>A
AA Mutation	p.Ala299Thr(p.A299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245312
Start	103051380:103051380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765181697
CDS Mutation	c.638G>A
AA Mutation	p.Gly213Glu(p.G213E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript