Colon Cancer: Gene >> SRPX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373004
Start	100650800:100650800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374870686
CDS Mutation	c.98C>T
AA Mutation	p.Pro33Leu(p.P33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373004
Start	100669272:100669272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370685595
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Trp(p.R374W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373004
Start	100662365:100662365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353G>A
AA Mutation	p.Arg118Lys(p.R118K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373004
Start	100664787:100664787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370296491
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373004
Start	100670896:100670896(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1311delC
AA Mutation	p.Glu438ArgfsTer12(p.E438Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373004
Start	100650783:100650783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SRPX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373004
Start	100665301:100665301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>T
AA Mutation	p.Glu197Asp(p.E197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript