Colon Cancer: Gene >> ADD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2914897:2914897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775330429
CDS Mutation	c.1619C>T
AA Mutation	p.Thr540Met(p.T540M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2884529:2884529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373A>G
AA Mutation	p.Thr125Ala(p.T125A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2876042:2876042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>T
AA Mutation	p.Pro43Ser(p.P43S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2898227:2898227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785C>T
AA Mutation	p.Ala262Val(p.A262V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2898446:2898446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202124018
CDS Mutation	c.899G>A
AA Mutation	p.Arg300Gln(p.R300Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2926071:2926071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1820T>C
AA Mutation	p.Val607Ala(p.V607A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2904926:2904926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324C>T
AA Mutation	p.Arg442Trp(p.R442W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2884582:2884582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426G>T
AA Mutation	p.Glu142Asp(p.E142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2894035:2894035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533A>G
AA Mutation	p.Glu178Gly(p.E178G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2904945:2904945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343T>C
AA Mutation	p.Leu448Pro(p.L448P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398129
Start	2928415:2928415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34737322
CDS Mutation	c.2106C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398129
Start	2914958:2914958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398129
Start	2907757:2907757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1428T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398129
Start	2928458:2928458(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746468920
CDS Mutation	c.2153delA
AA Mutation	p.Lys718ArgfsTer11(p.K718Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398129
Start	2894699:2894699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140019569
CDS Mutation	c.709G>A
AA Mutation	p.Val237Ile(p.V237I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398129
Start	2898228:2898228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786G>A
Mutation Classification	Silent
Feature Type	Transcript