Colon Cancer: Gene >> ABI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49217808:49217808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778504447
CDS Mutation	c.355C>T
AA Mutation	p.Pro119Ser(p.P119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49219919:49219919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771548372
CDS Mutation	c.610G>A
AA Mutation	p.Ala204Thr(p.A204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49222138:49222138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Asp284Tyr(p.D284Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49216664:49216664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774034002
CDS Mutation	c.251G>A
AA Mutation	p.Arg84Gln(p.R84Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49216582:49216582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>A
AA Mutation	p.Ala57Thr(p.A57T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49219600:49219600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>A
AA Mutation	p.Ala175Thr(p.A175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49222630:49222630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201030368
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339His(p.R339H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225941
Start	49222658:49222658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368794979
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225941
Start	49217772:49217772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225941
Start	49210811:49210811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770107994
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225941
Start	49222577:49222577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ABI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49216567:49216567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200111501
CDS Mutation	c.154G>A
AA Mutation	p.Ala52Thr(p.A52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225941
Start	49222608:49222608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994G>A
AA Mutation	p.Gly332Ser(p.G332S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225941
Start	49217855:49217855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript