Colon Cancer: Gene >> SRPX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38174312:38174312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771233820
CDS Mutation	c.197A>T
AA Mutation	p.Asp66Val(p.D66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38171899:38171899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375318852
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Trp(p.R170W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38172016:38172016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391T>C
AA Mutation	p.Phe131Leu(p.F131L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38164853:38164853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38174246:38174246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761387679
CDS Mutation	c.263G>A
AA Mutation	p.Arg88His(p.R88H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38160179:38160179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793C>A
AA Mutation	p.Leu265Ile(p.L265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378533
Start	38161031:38161031(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.677delC
AA Mutation	p.Pro226GlnfsTer32(p.P226Qfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000378533
Start	38160042:38160042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930G>A
AA Mutation	p.Trp310Ter(p.W310*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000378533
Start	38149884:38149884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222C>T
AA Mutation	p.Arg408Ter(p.R408*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000378533
Start	38172052:38172052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747378859
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Ter(p.R119*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SRPX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378533
Start	38174220:38174220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289G>A
AA Mutation	p.Gly97Ser(p.G97S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378533
Start	38160192:38160192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780A>G
Mutation Classification	Silent
Feature Type	Transcript