Colon Cancer: Gene >> AVIL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57803273:57803273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936G>A
AA Mutation	p.Val646Met(p.V646M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57810829:57810829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>T
AA Mutation	p.Gly182Val(p.G182V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57803596:57803596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745T>C
AA Mutation	p.Val582Ala(p.V582A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57807374:57807374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769888107
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483His(p.R483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57806466:57806466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768679508
CDS Mutation	c.1565A>C
AA Mutation	p.Lys522Thr(p.K522T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57811108:57811108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139710395
CDS Mutation	c.358G>A
AA Mutation	p.Ala120Thr(p.A120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257861
Start	57808495:57808495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755966655
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257861
Start	57813316:57813316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767162643
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257861
Start	57797981:57797981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2361A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257861
Start	57802295:57802295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2016T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AVIL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257861
Start	57814196:57814196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192714655
CDS Mutation	c.97G>A
AA Mutation	p.Ala33Thr(p.A33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript