Colon Cancer: Gene >> SPNS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28981996:28981996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28981509:28981509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703T>C
AA Mutation	p.Phe235Leu(p.F235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28983805:28983805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750776330
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447Gln(p.R447Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28982523:28982523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773924844
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28983909:28983909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138506930
CDS Mutation	c.1444G>A
AA Mutation	p.Ala482Thr(p.A482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28984216:28984216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201744028
CDS Mutation	c.1504G>A
AA Mutation	p.Glu502Lys(p.E502K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311008
Start	28981542:28981542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759504146
CDS Mutation	c.736G>A
AA Mutation	p.Val246Met(p.V246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311008
Start	28979223:28979223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372768895
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311008
Start	28981520:28981520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311008
Start	28979238:28979238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749187043
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPNS1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311008
Start	28977987:28977987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778204826
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript