Colon Cancer: Gene >> APPL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258530
Start	105208167:105208167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202080524
CDS Mutation	c.406G>A
AA Mutation	p.Ala136Thr(p.A136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258530
Start	105189817:105189817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414A>G
AA Mutation	p.Asn472Asp(p.N472D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258530
Start	105199457:105199457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772596522
CDS Mutation	c.779C>G
AA Mutation	p.Ser260Cys(p.S260C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258530
Start	105176961:105176961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727T>C
AA Mutation	p.Val576Ala(p.V576A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258530
Start	105203774:105203774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766770728
CDS Mutation	c.633T>A
AA Mutation	p.Phe211Leu(p.F211L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258530
Start	105199429:105199429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778171571
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258530
Start	105197821:105197821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258530
Start	105188386:105188386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1521C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258530
Start	105190053:105190053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750188627
CDS Mutation	c.1344G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258530
Start	105195281:105195281(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1221delA
AA Mutation	p.Lys407AsnfsTer11(p.K407Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000258530
Start	105199479:105199479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>T
AA Mutation	p.Glu253Ter(p.E253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000258530
Start	105188271:105188271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1634+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> APPL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258530
Start	105188418:105188418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536236110
CDS Mutation	c.1489C>T
AA Mutation	p.Arg497Trp(p.R497W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000258530
Start	105199479:105199479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>T
AA Mutation	p.Glu253Ter(p.E253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript