Colon Cancer: Gene >> WASF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26642302:26642302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145251421
CDS Mutation	c.32G>A
AA Mutation	p.Arg11Gln(p.R11Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26676613:26676613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749653652
CDS Mutation	c.605G>A
AA Mutation	p.Arg202His(p.R202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26665059:26665059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165G>T
AA Mutation	p.Leu55Phe(p.L55F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26685718:26685718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382G>T
AA Mutation	p.Arg461Leu(p.R461L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335327
Start	26671988:26671988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539A>G
AA Mutation	p.Lys180Arg(p.K180R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26681182:26681182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770387834
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26681118:26681118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>A
AA Mutation	p.Gln261Lys(p.Q261K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26685703:26685703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367A>G
AA Mutation	p.Lys456Arg(p.K456R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26682660:26682660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759410889
CDS Mutation	c.1037C>T
AA Mutation	p.Pro346Leu(p.P346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26671920:26671920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471C>A
AA Mutation	p.Phe157Leu(p.F157L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26685735:26685735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758369538
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Trp(p.R467W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335327
Start	26685821:26685821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757100402
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335327
Start	26681262:26681262(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.929delC
AA Mutation	p.Pro310LeufsTer25(p.P310Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335327
Start	26685699:26685699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1367delA
AA Mutation	p.Lys456ArgfsTer61(p.K456Rfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WASF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26642376:26642376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>A
AA Mutation	p.Ala36Thr(p.A36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335327
Start	26665097:26665097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203C>A
AA Mutation	p.Ser68Tyr(p.S68Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335327
Start	26685824:26685824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335327
Start	26682868:26682868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148684191
CDS Mutation	c.1245G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335327
Start	26667539:26667540(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.297dupA
AA Mutation	p.Ala100SerfsTer20(p.A100Sfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript