Colon Cancer: Gene >> SPRED2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65344808:65344808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115A>G
AA Mutation	p.Ser39Gly(p.S39G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65314081:65314081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754327382
CDS Mutation	c.677C>T
AA Mutation	p.Thr226Met(p.T226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65314130:65314130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628G>A
AA Mutation	p.Asp210Asn(p.D210N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65313863:65313863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Trp(p.R299W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65313656:65313656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>A
AA Mutation	p.Asp368Asn(p.D368N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65313535:65313535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1223G>T
AA Mutation	p.Arg408Met(p.R408M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65313548:65313548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374710787
CDS Mutation	c.1210G>A
AA Mutation	p.Gly404Arg(p.G404R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65344880:65344880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749197715
CDS Mutation	c.43C>T
AA Mutation	p.Arg15Cys(p.R15C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65334621:65334621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65313582:65313582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65313687:65313687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761279539
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65344815:65344815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65313594:65313594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65313573:65313573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65314035:65314035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPRED2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356388
Start	65313868:65313868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890C>T
AA Mutation	p.Ser297Leu(p.S297L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356388
Start	65314116:65314116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151327457
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript