Colon Cancer: Gene >> SPNS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4530735:4530735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202089427
CDS Mutation	c.677C>T
AA Mutation	p.Thr226Met(p.T226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4536122:4536122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1391G>A
AA Mutation	p.Ser464Asn(p.S464N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4536365:4536365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1546G>A
AA Mutation	p.Gly516Ser(p.G516S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4536278:4536278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759860679
CDS Mutation	c.1459C>T
AA Mutation	p.Arg487Cys(p.R487C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4532561:4532561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812T>C
AA Mutation	p.Met271Thr(p.M271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4536410:4536410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200121169
CDS Mutation	c.1591G>A
AA Mutation	p.Ala531Thr(p.A531T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329078
Start	4530766:4530766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199620984
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329078
Start	4530674:4530674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.619delG
AA Mutation	p.Glu207ArgfsTer46(p.E207Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329078
Start	4536336:4536345(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1518_1527delGCTCTGCCCT
AA Mutation	p.Met506IlefsTer29(p.M506Ifs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPNS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329078
Start	4530767:4530767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767740179
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329078
Start	4536316:4536316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497G>A
Mutation Classification	Silent
Feature Type	Transcript