Colon Cancer: Gene >> WASL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123704651:123704651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>T
AA Mutation	p.Arg148Ile(p.R148I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000223023
Start	123706742:123706742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>T
AA Mutation	p.Asp113Tyr(p.D113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123696624:123696624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>C
AA Mutation	p.Lys195Thr(p.K195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123706291:123706291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Arg141Gln(p.R141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123684523:123684523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514A>G
AA Mutation	p.Asp505Gly(p.D505G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123694825:123694825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716G>A
AA Mutation	p.Cys239Tyr(p.C239Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123684526:123684526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1511A>G
AA Mutation	p.Glu504Gly(p.E504G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123709120:123709120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221G>T
AA Mutation	p.Arg74Ile(p.R74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123692621:123692621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073C>A
AA Mutation	p.Pro358His(p.P358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123694832:123694832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>A
AA Mutation	p.Asp237Asn(p.D237N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223023
Start	123692536:123692536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368113473
CDS Mutation	c.1158G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223023
Start	123709152:123709152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223023
Start	123696593:123696593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223023
Start	123706755:123706755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223023
Start	123692431:123692431(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1263delA
AA Mutation	p.Val422TrpfsTer17(p.V422Wfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000223023
Start	123706322:123706322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Ter(p.R131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000223023
Start	123692370:123692370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324C>T
AA Mutation	p.Arg442Ter(p.R442*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WASL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123706321:123706321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200364266
CDS Mutation	c.392G>A
AA Mutation	p.Arg131Gln(p.R131Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223023
Start	123706291:123706291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Arg141Gln(p.R141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000223023
Start	123696649:123696649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559G>T
AA Mutation	p.Glu187Ter(p.E187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript