Colon Cancer: Gene >> ADD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70706395:70706395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Thr5Met(p.T5M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70672886:70672886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862C>T
AA Mutation	p.Ser621Phe(p.S621F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70677829:70677829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Cys(p.R478C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70663549:70663549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377717831
CDS Mutation	c.2057C>T
AA Mutation	p.Ser686Leu(p.S686L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70678823:70678823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264C>T
AA Mutation	p.His422Tyr(p.H422Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70678714:70678714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373C>A
AA Mutation	p.Pro458His(p.P458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70683640:70683640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370464708
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359Gln(p.R359Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70690818:70690818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817A>G
AA Mutation	p.Asn273Asp(p.N273D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264436
Start	70678705:70678705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758903259
CDS Mutation	c.1382C>T
AA Mutation	p.Thr461Met(p.T461M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70678780:70678780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201022450
CDS Mutation	c.1307C>T
AA Mutation	p.Thr436Met(p.T436M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70677802:70677802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1459C>T
AA Mutation	p.Pro487Ser(p.P487S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70706402:70706402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200519011
CDS Mutation	c.7G>A
AA Mutation	p.Glu3Lys(p.E3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70683725:70683725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991C>A
AA Mutation	p.Leu331Ile(p.L331I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70677807:70677807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1454T>G
AA Mutation	p.Phe485Cys(p.F485C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70692455:70692455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782189292
CDS Mutation	c.653C>T
AA Mutation	p.Ala218Val(p.A218V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264436
Start	70706376:70706376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264436
Start	70663674:70663674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115476558
CDS Mutation	c.1932G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264436
Start	70676814:70676814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201133279
CDS Mutation	c.1575C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264436
Start	70704370:70704370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782016516
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70706317:70706317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92A>G
AA Mutation	p.Tyr31Cys(p.Y31C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70663684:70663684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1922C>G
AA Mutation	p.Thr641Arg(p.T641R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264436
Start	70696327:70696327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392G>A
AA Mutation	p.Arg131Gln(p.R131Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript